HERMES: Hemodynamic Resuscitation and Monitoring in Early Sepsis

Sponsor
Tata Memorial Centre (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04143035
Collaborator
Indian Society of Critical Care Medicine (Other)
500
248
32.4
2
0.1

Study Details

Study Description

Brief Summary

"Hemodynamic Resuscitation and Monitoring in Early Sepsis (HERMES Study)" involves recording of patient's medical data related to that has been collected as part of his/her routine medical care in ICU.

Presently there is no data from Indian ICUs on the way patients in early sepsis are resuscitated and monitored. There may exist a wide variation in clinical practice. The investigators would like to conduct an observational study in various levels of Indian ICUs, to prospectively collect data on adult patients admitted to ICU with early sepsis in a 60-day window period. Investigator would like to study the hemodynamic resuscitation and monitoring performed in these patients. In addition, Investigator would like to identify factors associated with improved outcomes and achieving the goals of the sepsis bundles in one, three and six hours.

The objectives of the study is to capture the patient characteristics and hemodynamic resuscitation and monitoring practices in patients presenting with early sepsis and hypotension to Indian ICUs

Investigator plan to recruit 50 -100 centers nationwide. Each center will be asked to collect data from at least 10 patients in a maximum time window of 60 days. A convenience sample of minimum 500 patients presenting to ICU with suspected sepsis and hypotension will be taken.

Each Centre will guarantee the integrity of data collection and ensure timely completion of the case record forms. Each center will select a 60 day window period for patient recruitment. The start date may be anytime any time between 1st August to 15th October 2019. Therefore, the recruitment window period will end for a respective centre, anytime between 30th September and 14th December 2019, depending on the start date. All consecutive patients in the 60-day period will be screened and those eligible will be enrolled.

This is an ISCCM(Indian Society of Critical Care Medicine) Research Committee funded study. The ISCCM will fund the Principal Investigator for all expenses related software development, website hosting, secretarial assistance and miscellaneous expenses related to the conduct of the study, data analysis and publication. No funding will be given to the investigators from the various participating centers for contributing data.

Condition or Disease Intervention/Treatment Phase
  • Other: No Intervention

Detailed Description

INTRODUCTION Septic shock is the most commonly occurring of all types of shock.The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3) defines septic shock as a subset of sepsis in which particularly profound circulatory, cellular, and metabolic abnormalities are associated with a greater risk of mortality than with sepsis alone. Patients with septic shock can be clinically identified by a vasopressor requirement to maintain a mean arterial pressure of 65 mm Hg or greater and serum lactate level greater than 2 mmol/L (>18 mg/dL) in the absence of hypovolemia. This combination is associated with hospital mortality rates greater than 40%.

The "sepsis bundle" has been central to the implementation of the Surviving Sepsis Campaign (SSC) from the first publication of its evidence-based guidelines in 2004 through subsequent editions. Developed separately from the guidelines publication by the SSC, the bundles have been the cornerstone of sepsis quality improvement since 2005. An updated version was published in 2016 "Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock". There is compelling nature of the evidence in the literature which demonstrates an association between compliance with bundles and improved survival in patients with sepsis and septic shock. This has led to the adoption of the SSC measures by the National Quality Forum (NQF) and other departments. The important relationship between the bundles and survival was confirmed in a publication from this initiative.

The Surviving Sepsis Campaign released an updated one-hour sepsis bundle, which combines recommendations listed in the three-hour and six-hour bundles. This includes 5 elements: 1. measuring lactate levels 2. obtaining blood cultures before administering antibiotics 3. administering broad-spectrum antibiotics 4. fluid resuscitation for hypotension or lactate level ≥ 4 mmol/L and 5. use of vasopressors for hypotensive during or after fluid resuscitation to maintain MAP ≥ 65 mm Hg.

Presently there is no data from Indian ICUs on the way patients in early sepsis are resuscitated and monitored. There may exist a wide variation in clinical practice.The Investigator would like to conduct an observational study in various levels of Indian ICUs, to prospectively collect data on adult patients admitted to ICU with early sepsis in a 60-day window period. Investigator would like to study the hemodynamic resuscitation and monitoring performed in these patients. In addition, investigator would like to identify factors associated with improved outcomes and fulfilling the goals of the one hour SSC bundles within one, three and six hours in patients with sepsis and septic shock.

OBJECTIVES

  1. To capture the patient characteristics and hemodynamic resuscitation and monitoring practices in patient presenting with early sepsis and hypotension to Indian ICUs

  2. To determine various factors associated with improved survival in patients with septic shock

  3. To determine factors associated with achieving the 1 hour, 3 hour and 6-hour resuscitation goals of the sepsis bundle in patients with septic shock

METHODS Study design- Prospective observational multi-center national cohort study.

Patient Recruitment

ISCCM members across India will be contacted to register their ICUs in the study, through emails sent from the ISCCM Research committee. Repeated emails will be sent over a two-month period. Hospitals with more than one ICU can enroll each of their ICUs separately. Each ICU will need to contribute a minimum of 10 adult patients with sepsis and hypotension in a 60 day window period.

Each center will designate a maximum of two local coordinators (PI and Co-PI) who will provide scientific and structural leadership in their centers. They will ensure that all local necessary ethical and regulatory approvals are obtained before the start of patient inclusion.

Local coordinators will guarantee the integrity of data collection and ensure timely completion of the case record forms. Each center will select a 60 day window period for patient recruitment. The start date may be anytime any time between 1st August to 15th October 2019. Therefore, the recruitment window period will end for a respective centre, anytime between 30th September and 14th December 2019, depending on the start date. All consecutive patients in the 60-day period will be screened and those eligible will be enrolled.

Data Collection

  1. There will be no direct patient contact or intervention. Local coordinators will guarantee the integrity of data collection and ensure timely completion of CRFs (case record forms). Date related to the following will be collected prospectively from the charts:

  2. Patient demographic data e.g. age, sex, comorbidities, likely source of sepsis

  3. Total number of ICU patients, patients with sepsis and septic shock admitted to the ICU in the 60 days period

  4. Patient clinical examination findings and severity of illness

  5. Details of hemodynamic monitoring and other systemic monitoring and therapy performed in ICU e.g. fluid bolus, vasopressor agents, monitoring devices used, hemodynamic variables measured, mechanical ventilation, dialysis etc. in the first 3 days of ICU admission

  6. Antibiotics administered and details of microbiology examinations

  7. Adjunct therapies initiated for sepsis

  8. ICU, hospital and 28-day mortality

Sample size The primary endpoint of study was to determine the incidence of ICU mortality in patients with septic shock admitted to Indian ICUs. The sample size calculation was done on the basis of INDICAPS I(Indian Intensive Care Case Mix and Practice Patterns Study-I) Study data (IJCCM April 2016). In this study the ICU mortality incidence was found to be 45% in patients with septic shock. Assuming the incidence rate found in this study, a sample size of 401 produces a two-sided 95% confidence interval with a width equal to 0.100 when the sample proportion is 0.450. Sample size calculation was done using PASS software. To account for attrition, Investigator will take a sample size of at least 450 patients. Investigator plan to recruit 50 -100 centers nationwide. Each center will be asked to collect data from at least 10 patients, hence investigator should be able to meet this target of >450 patients.

Statistical analysis The primary objective of the study is to determine the patient characteristics and hemodynamic resuscitation and monitoring practices in patient presenting with early sepsis and hypotension to Indian ICUs which will be analyzed using descriptive statistics. To determine various factors associated with improved survival in patients with septic shock investigator will use the Fisher's exact test or Pearson's χ2 test. Univariable and Multivariable logistic regression models will be developed to assess the independent effects on ICU mortality. To determine factors associated with achieving the 1 hour SSC Sepsis resuscitation bundle in 1 hour, 3 hours and 6-hours in patients with sepsis and septic shock will be assessed by Fisher's exact test or Pearson's χ2 test. Univariable and Multivariable logistic regression models will be developed to assess the independent effects on ICU mortality of the 1 hour, 3 hour and 6-hour resuscitation goals of the sepsis bundle in patients with sepsis and septic shock. The overall performance of the internally validated model will be assessed using Nagelkerke's R2 (R squared in logistic regression). The higher Nagelkerke's R2, the greater the strength of the model. The ability of the models to identify ICU mortality will be quantified as the area under the receiver operating characteristic curve (AUC). The AUC ranges from 50% to 100%, indicating no discriminative capacity to perfect discriminative capacity. The agreement between predicted probabilities and observed frequencies of the outcome will be assessed by visually inspecting the calibration plot. Last, the Hosmer and Lemeshow goodness-of-fit statistic will be computed as a quantitative measure of accuracy. A high outcome of this statistic is related to a low p-value, which indicates a poor fit. All analysis will two sided, and significance will set at a p-value of 0.05. Statistical analyses will be performed using SPSS (the statistical package for social sciences) IBM Corp. Released 2017. IBM SPSS Statistics for Windows, Version 25.0. Armonk, New York: IBM Corp and R studio (version 1.2).

INSTITUTIONAL ETHICS COMMITTEE (IEC) APPROVAL The local hospital investigators should ensure that all necessary local ethical and regulatory approvals are obtained if required, before the start of the study in their institution.

CONSENT FOR DATA COLLECTION This is an observational study and involves capture of data from the patient charts. There is no direct patient contact or intervention, hence written, informed consent is not mandatory. However, if required by the institution, consent may be taken from the patients legally accepted representative (LAR). Sample short consent forms for patient data capture will be provided by the PI in English, Hindi and Marathi. This may be translated in various regional languages as required by the local investigator

STUDY FUNDING This is an ISCCM Research Committee funded study. The ISCCM will fund the Principal Investigator institution for all expenses related software development, website hosting, secretarial assistance and miscellaneous expenses related to the conduct of the study, data analysis and publication (against actual bills). No funding will be given to the investigators from the various participating centres for contributing data.

DATA STORAGE AND OWNERSHIP The Principal Investigator will have ownership of the data. The data will be stored in the Principal Investigators department at Tata Memorial Hospital, Mumbai for 10 years.

PUBLICATION AND AUTHORSHIP POLICY The main results of study will be published in a peer-reviewed medical journal. Authorship policy will follow the International Committee of Medical Journal Editors (ICMJE) recommendations. Authorship will be considered based on contributions the study design and protocol development, recruitment of patients, data acquisition and cleaning, analysis and interpretation of the data, manuscript writing and final approval of the version to be published and agreement to be accountable for all aspects of the work, in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Steering Committee - Members of the Steering Committee will include 7 members from the Principal Investigators center and 8 -10 experts from across the country. They will be involved and provide active guidance from inception till publication of the study.

Writing committee and main author list - Members of the steering committee and Principal Investigator from the top 3 centers with highest number of patient recruitment.

The Principal Investigator and Co-Principal Investigator from each participating ICU will be in the list of study collaborators and their names will be in the publication. The names of all the investigators will be indexed in PubMed depending on the journal policy.

SECONDARY ANALYSES After publication of the primary results, on request, the pooled dataset will be available for investigators for secondary analysis, after judgment and approval of scientific quality and validity by the steering committee. Before submission, the final version of all manuscripts related to the study dataset must be approved by the steering committee. The members of the writing committee will be authors of the publications derived from the study dataset.

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Hemodynamic Resuscitation and Monitoring in Early Sepsis
Actual Study Start Date :
Aug 1, 2019
Anticipated Primary Completion Date :
Apr 13, 2022
Anticipated Study Completion Date :
Apr 13, 2022

Outcome Measures

Primary Outcome Measures

  1. ICU Mortality [throughout ICU stay till discharge (up to 2 months)]

    Overall ICU Mortality due to septic shock with hypotension

  2. Completing the elements of the one hour SSC sepsis bundle in one 1 hour [1 hour after admission upto 60 days from the study start date in respective study site (60 days)]

    Identify factors associated with improved outcomes and fulfilling the goals of the one hour Surviving Sepsis Campaign (SSC) bundles within one, three and six hours in patients with sepsis and septic shock and to identify compliance with the one hour SSC bundle guidelines The Surviving Sepsis Campaign released an updated one-hour sepsis bundle, which combines recommendations listed in the three-hour and six-hour bundles. This includes 5 elements: 1. measuring lactate levels 2. obtaining blood cultures before administering antibiotics 3. administering broad-spectrum antibiotics 4. fluid resuscitation for hypotension or lactate level ≥ 4 mmol/L and 5. use of vasopressors for hypotensive during or after fluid resuscitation to maintain MAP ≥ 65 mm Hg

Secondary Outcome Measures

  1. Hospital mortality [throughout the hospital stay till discharge in the respective study site (up to 3 months)]

    Over all mortality during the hospital stay

  2. 28-day mortality [From ICU admission to 28 days in the respective study site (up to 3 months)]

    Over all mortality from ICU admission day to till 28 day

  3. Completing the elements of the one hour SSC sepsis bundle in one, three and six hours [1 hour, 3 hour and six hour after admission upto 60 days from the study start date in the respective study site (60 days )]

    Identify factors associated with improved outcomes and fulfilling the goals of the one hour Surviving Sepsis Campaign (SSC) bundles within one, three and six hours in patients with sepsis and septic shock and to identify compliance with the one hour, three hour and six hour SSC bundle guidelines The Surviving Sepsis Campaign released an updated one-hour sepsis bundle, which combines recommendations listed in the three-hour and six-hour bundles. This includes 5 elements: 1. measuring lactate levels 2. obtaining blood cultures before administering antibiotics 3. administering broad-spectrum antibiotics 4. fluid resuscitation for hypotension or lactate level ≥ 4 mmol/L and 5. use of vasopressors for hypotensive during or after fluid resuscitation to maintain MAP ≥ 65 mm Hg

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion criteria

  1. Adult patients (≥ 18 years old)

  2. Presenting to ICU with suspected sepsis

  3. Presence of hypotension (Systolic BP ≤ 90 mmHg / Mean arterial pressure (MAP) ≤ 65mmhg or patient with Systolic BP > 90 mmHg / MAP >65mmHg on vasopressor.

Exclusion Criteria

  1. Patient likely to be in shock due to reason other than sepsis (e.g. cardiogenic or hemorrhagic shock)

  2. Decision taken for not intubating / ventilating /aggressive resuscitation prior to ICU admission

  3. Patient transferred from another ICU OR another hospital (only if stay >7 days)

Contacts and Locations

Locations

Site City State Country Postal Code
1 AIIMS Patna Patna Bihar India
2 All india institute of medical sciences Patna Bihar India
3 Anant Institute of Medical Sciences Jabalpur Madhya Pradesh India
4 Breach Candy Hospital Trust Mumbai Maharashtra India
5 Criticare Hospital and Research Institute Nagpur Maharashtra India
6 Galaxy care hospital Pune Maharashtra India
7 Sanjeevan Hospital Pune Maharashtra India
8 Dayanand Medical College and Hospital Ludhiyana Panjab India
9 Eternal Hospital Jaipur Rajasthan India
10 Kamlesh Kanwar Shekhawat Udaipur, Rajasthan India
11 Pims Udaipur Rajasthan India
12 Sarvodaya hospital and research centre Faridabad Uttar Pradesh India
13 Fortune Hospital Kanpur Uttar Pradesh India
14 Sir Sundar lal Hospital, IMS, BHU, Varanasi Varanasi Uttar Pradesh India
15 Sir Sunderlal Hospital Varanasi Uttar Pradesh India
16 Nayati Hospital - Trauma & Acute Care Centre Agra India
17 Purushottam das Savitri Devi Cancer center Agra India
18 Pushpanjali Hospital Agra India
19 Rainbow Hospitals Agra India
20 Narayana Multispeciality Hospital Ahmedabad India
21 Sterling hospital Ahmedabad India
22 Zydus Hospitals Ahmedabad Ahmedabad India
23 Saideep Healthcare and Research Pvt Ltd Ahmednagar India
24 J N Medical College & Hospital Alīgarh India
25 Ohm Trauma centre and critical care Alīgarh India
26 Emc hospital Amritsar India
27 Fortis Escorts Hospital Amritsar Amritsar India
28 Kamalnayan Bajaj hospital Aurangabad India
29 Mgm Medical College Hospital and Medical Centre Research Institute(McRi) Aurangabad India
30 Oriion Citicare Superspeciality Hospital Aurangabad India
31 Shraddha hospital and critical care center Aurangabad India
32 Bhagwan Mahaveer Jain Hospital Bangalore India
33 Columbiaasia Referral Hospital, Yeshwantpur Bangalore India
34 Cytecare Cancer Hospital Bangalore India
35 Health care Global (HCG) Bangalore India
36 Shifaa hospital Bangalore India
37 Shri Ram Murti Smarak Institute of Medical Sciences Bareilly India
38 Geeta Hospital and research centre Barnagar India
39 Aster R V Hospital Bengaluru India
40 Manipal hospital Bengaluru India
41 Mazumdar Shaw Medical Center Bengaluru India
42 Regal Hospital Bengaluru India
43 St John's Medical College Hospital Bengaluru India
44 Vydehi Institute of Medical Sciences and Research Centre Bengaluru India
45 Apollo Hospitals Bhubaneshwar India
46 Amri hospital ICU -1 Bhubaneswar India
47 AMRI Hospitals Bhubaneswar India
48 Amri Hospital Bhubaneswar India
49 Apollo Hospitals Bhubaneswar India
50 Apollo Hospital Bhubaneswar India
51 BR Life Kalinga Hispital Bhubaneswar India
52 Care Hospitals Bhubaneswar India
53 Care Hospital Bhubaneswar India
54 Gudage Hospital Bidar India
55 Ayush Hospital Bijapur India
56 Apollo Hospital Icu-1 Bilaspur India
57 Apollo Hospital Bilaspur India
58 K.M.Memorial hospital and research centre Bokāro India
59 PGIMER Chandigarh India
60 Apollo Hospitals Enterprise limited Chennai India
61 Billroth hospital Chennai India
62 Dr.Rela Institute and Medical Centre Chennai India
63 Mgm Healthcare Ltd. Chennai India
64 Sri Ramachandra Hospital Chennai India
65 Sri Ramchandra Medical Centre Chennai India
66 MOSC Medical College Cochin India
67 Kovai Medical Center Hospital and Research Coimbatore India
68 Royal Care Super Speciality Hospital Coimbatore India
69 Ashwini Hospital Cuttack India
70 Goodluck Hospital Cuttack India
71 Scb Medical College and Hospital Cuttack India
72 SCB Medical College Cuttack India
73 Paras Global Hospital Darbhanga India
74 Dharmshila Narayana Superspeciality Hospital Delhi India
75 Dr. Ram Manohar Lohia Hospital ,New Delhi Delhi India
76 Dr. Ram Manohar Lohia Hospital Delhi India
77 kailash Hospital and heart Institute Delhi India
78 Pushpawati Singhania Research Institute Delhi India
79 Sir Ganga Ram Hospital Delhi India
80 BKL Walawalkar Hospital Dervan India
81 Muthukrishnan Periasamy Erode India
82 Qrg Healthcity Faridabad India
83 Yashoda super specialty hospital, kaushambi Ghāziābād India
84 City Hospital Gorakhpur India
85 Dr.Ramesh Cardiac and Multiplicity PVT LTD Guntur India
86 GBR super speciality hospitals Guntur India
87 Lalitha Super Specialities Hospital Guntur India
88 Samistha Hospital and Research Institute Guntur India
89 Medanta Medicity Gurgaon India
90 Medanta the medicity hospital Gurgaon India
91 Medanta the medicity Gurgaon India
92 Narayana Super Specialty Hospital Gurgaon India
93 VPS Medeor Hospital Gurgaon India
94 Apollo Hospitals Guwahati Guwahati India
95 Apollo hospitals Guwahati India
96 Ayursundra Superspecialty hospital Guwahati India
97 Dispur Hospitals pvt Ltd Guwahati India
98 Gnrc Hospitas, Dispur Guwahati India
99 Health City Guwahati India
100 Nemcare Hospital Guwahati India
101 Santhi Hospital Hosur India
102 Aig Hospitals, Gachibowli Hyderabad India
103 Apollo Health City ICU-1 Hyderabad India
104 Apollo health city Hyderabad India
105 Aware Gleneagles Global Hospital Hyderabad India
106 Care hospital and institute of medical sciences Hyderabad India
107 Care hospitals banjara Hyderabad India
108 CENTURY hospital Hyderabad India
109 Century Super Speciality Hospital Hyderabad India
110 Continental Hospitals Hyderabad India
111 Gleneagles Global Hospital Hyderabad India
112 Krishna Institute of Medical Sciences Hyderabad India
113 Rainbow childrnes hospital Hyderabad India
114 South Central Railway Hospital ICU-1 Hyderabad India
115 South Central Railway Hospital Hyderabad India
116 Virinchi Hospital Hyderabad India
117 Yashoda Hospital Hyderabad India
118 Choithram hospital Indore India
119 Dodeja Hospital Jabalpur India
120 Apex Hospital Jaipur India
121 Manipal hospital Jaipur India
122 Shubh Hospital Jaipur India
123 shrimann superspeciality hospital ICU-1 Jalandhar India
124 Shrimann Superspeciality Hospital Jalandhar India
125 Kripa Critical Care and Trauma Centre Jalgaon India
126 Smvd Narayana Superspeciality Hospital Jammu India
127 Tata Main Hospital Jamshedpur India
128 All India Institute of Medical Sciences, jodhpur Jodhpur India
129 Ved Hospital Kalyan India
130 Abha superspeciality hospital Kanpur India
131 Regency hospital ltd tower 1 Kanpur India
132 Shree krishna hospital ICU-1 Karamsad India
133 Shree Krishna Hospital Karamsad India
134 Sankalpa hospital Khammam India
135 Amrita institute of Medical Sciences Kochi India
136 AMRI Hospital Mukundapur Kolkata India
137 AMRI Hospital, DHAKURIA Kolkata India
138 Apollo Gleneagles Hospital Kolkata India
139 Bellevue Clinic Kolkata India
140 Fortis Hospital Anandapur Kolkata India
141 Institute of Neurosciences Kolkata Kolkata India
142 Medica Superspecialty Hospital Kolkata India
143 Peerless Hospitex Hospital and Research Center Limited Kolkata India
144 Tata Medical Center Kolkata India
145 Travancore medical college,medicity Kollam India
146 Govt.Medical college Kottayam India
147 King George's Medical University Lucknow India
148 Christian Medical College Ludhiana India
149 Apollo speciality hospital Madurai India
150 Kasturba medical college, Manipal Manipala India
151 Nayati medicity hospital Mathura India
152 Manglam Hosp Meerut India
153 Metro Hospital and heart Institute Meerut India
154 Cheema Medical Complex Mohali India
155 Fortis Hospital Mohali India
156 MAX Superspecialty Hospital Mohali India
157 Asian Cancer Institute Mumbai India
158 Bhatia Hospital Mumbai India
159 Dr L H HIRANANDANI HOSPITAL Mumbai India
160 Fortis hiranandani hospital Mumbai India
161 Fortis Hospital Mulund Mumbai India
162 Fortis hospitals Mumbai India
163 Global Hospital,Parel Mumbai India
164 Global Hospital Mumbai India
165 Holy Family Hospital Mumbai India
166 Nanavati Hospital Icu-1 Mumbai India
167 Nanavati hospital ICU-2 Mumbai India
168 Nanavati Hospital Icu-3 Mumbai India
169 Nanavati Hospital Mumbai India
170 Nanavati hosptial Mumbai India
171 Pd Hinduja National Hospital and Mrc Mumbai India
172 s.l.Rahej hospital- a fortis associate Mumbai India
173 Sir H N Reliance Foundation Hospital Mumbai India
174 Suasth Health Care Mumbai India
175 Tata Memorial Hospital (FICU) Mumbai India
176 Tata Memorial Hospital (SICU) Mumbai India
177 Wockhardt Hopsital South Mumbai Mumbai India
178 Cauvery Heart and multispeciality hospital Mysore India
179 Jss Hospital Mysore India
180 Gopalagowda Shanthaveri Memorial Hospital Mysuru India
181 Aditya Hospital Nagpur India
182 Dew medicare and Trinity Hospital Nagpur India
183 Dr V E Tambe Critical Care Nagpur India
184 Meditrina Institute Of Medical Scineces Nagpur India
185 Orange City Hospital And Research Institute Nagpur India
186 Rahate Surgical Hospital and Iccu Nagpur India
187 Shree Hospital and Critical Care Centre Nagpur India
188 Apollo Hospitals Nashik India
189 National Burns Centre Navi Mumbai India
190 Simhapuri Hospital Nellore, India
191 Narayana Medical College Icu-1 Nellore India
192 Narayana Medical College Nellore India
193 Batra Hospital & Medical Research Center New Delhi India
194 Batra Hospital New Delhi India
195 BLK hospital New Delhi India
196 Blk Superspeciality Hospital New Delhi India
197 Fortis Escorts Heart Institute New Delhi India
198 Fortis Hospital, Shalimar Bagh New Delhi India
199 GB Pant Institute of Post Graduate Medical Education & Research New Delhi India
200 Indraprastha Apollo Hospitals ICU-1 New Delhi India
201 Indraprastha apollo hospitals New Delhi India
202 Max Super Specialty Hospital Patparganj New Delhi India
203 Northern railway central hospital New Delhi India
204 Sri balaji action medical institute ICU-1 New Delhi India
205 Sri Balaji Action Medical Institute New Delhi India
206 Venkateshwar Hospital New Delhi India
207 Fortis Hospital Noida India
208 Promhex Multispeciality Hospital Noida India
209 Ojas hospital Panchkula India
210 All India Institute of Medical Sciences Patna Patna India
211 Indira Gandhi Institute of Medical Sciences Patna India
212 Prabhat Kumar Patna India
213 Bharati Vidyapeeth Deemed university and Medical College Hospital Pune India
214 Columbia Asia hospital Pune India
215 Jupiter Hospital Pune India
216 Niramaya Hoapital Pune India
217 Ruby Hall Clinic Icu-1 Pune India
218 Ruby Hall Clinic ICU-2 Pune India
219 Vishwaraj Hospital & Research Centre Pune India
220 Vishwaraj Hospital& Research Center Pune India
221 Om Hospital Raipur India
222 Pt. J. N. M. Medical College Raipur India
223 Ramskrishna care hospital Raipur India
224 Shree Narayana Hospital Raipur India
225 Genesis Multispeciality Hospital Rajkot India
226 Shree Giriraj Multispecialty Hospital Rajkot India
227 Sterling Hospital, Rajkot (A Division of Sterling Addlife India Private Limited) Rajkot India
228 Synergy superspeciality hospital Rajkot India
229 Bhagwan Mahavir Medica Superspecialty Hospital Ranchi India
230 Shree Giriraj Multispeciality hospital Rājkot India
231 Sagarshree Hospital Sagar India
232 Abdul Waheed Mir Srinagar India
233 Sheri Kashmir Institute of Medical Sciences Srinagar India
234 Kiran Hospital Surat India
235 Shree Sardar Smarak Hospital Surat India
236 Sagarshree Hospital Sāgar India
237 Believers Church Medical College and Hospital Tiruvalla India
238 Trichy Srm Medical College Hospital & Research Centre Trichinopoly India
239 Kerala Institute of Medical sciences Trivandrum India
240 Siddaganga hospital and research centre Tumuluru India
241 Sterling Hospitals Vadodara India
242 Homi Bhaba Cancer Hospital & Pandit Madan Mohan Malviya Cancer Centre,Tata Memorial Centre,Varanasi Varanasi India
243 S S Hospital BHU VARANASI Varanasi India
244 Christian Medical College Vellore India
245 Nagarjuna hospital Vijayawada India
246 St Ann Hospital Visakhapatnam India
247 Samraksha super speciality Warangal India
248 Arnam Hospital Wardha India

Sponsors and Collaborators

  • Tata Memorial Centre
  • Indian Society of Critical Care Medicine

Investigators

  • Principal Investigator: Sheila N Myatra, MD, Tata Memorial Hospital, Parel, Mumbai-12

Study Documents (Full-Text)

More Information

Additional Information:

Publications

Responsible Party:
Sheila Nainan Myatra, Professor, Tata Memorial Centre
ClinicalTrials.gov Identifier:
NCT04143035
Other Study ID Numbers:
  • 3364
First Posted:
Oct 29, 2019
Last Update Posted:
Oct 26, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 26, 2021