SevoCOPD: Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disease Patients

Sponsor
Employee's State Insurance Corporation, New Delhi (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06108973
Collaborator
Medtronic Spine LLC (Industry)
45
14.9

Study Details

Study Description

Brief Summary

All the Patients undergoing General Anesthesia and the patients who are having Chronic Obstructive Pulmonary Disease will be considered for this study. The Volume consumption of Sevoflurane will be studied in accordance with age, sex, duration , type of surgery, site of surgery and BMI.The volume consumption of sevoflurane is compared with Chronic Obstructive Pulmonary Disease and Normal Patients .

Condition or Disease Intervention/Treatment Phase
  • Device: Capnography

Detailed Description

Chronic Obstructive pulmonary disease is known to escalate the consumption of Inhalation Agents in General Anesthesia. Hence the Data to Collect the Official Record

Study Design

Study Type:
Observational
Anticipated Enrollment :
45 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disease Patients Under General Anesthesia
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
Dec 30, 2024
Anticipated Study Completion Date :
Mar 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Normal Patients

Normal patients without any Lung Pathology for General Anesthesia

Device: Capnography
To know the Co2 graph in COPD and Normal patients under General Anesthesia

COPD patients

Established Chronic Obstructive Pulmonary Disease for General Anesthesia

Device: Capnography
To know the Co2 graph in COPD and Normal patients under General Anesthesia

Outcome Measures

Primary Outcome Measures

  1. Estimation of Volume consumption of Sevoflurane [8 weeks]

    The consumption is expressed in Volume ml/kg

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Both Sex All Age Group Patient willing to give consent COPD patient
Exclusion Criteria:
  • Not willing to give consent Cancerous Lung Lung Lobectomy

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Employee's State Insurance Corporation, New Delhi
  • Medtronic Spine LLC

Investigators

  • Principal Investigator: Dr Manjunath, MD, ESIC

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Santhosh Kumar T N, Nursing Orderly, Employee's State Insurance Corporation, New Delhi
ClinicalTrials.gov Identifier:
NCT06108973
Other Study ID Numbers:
  • 00127102023
First Posted:
Oct 31, 2023
Last Update Posted:
Oct 31, 2023
Last Verified:
Oct 1, 2023
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:
Yes
Product Manufactured in and Exported from the U.S.:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 31, 2023