Impact of Early Antibiotics on Non-Traumatic Out of Hospital Cardiac Arrest (OHCA)

Sponsor
Hamad Medical Corporation (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT05914779
Collaborator
(none)
1,000
1
2
34
29.4

Study Details

Study Description

Brief Summary

Specific Aim : The specific aim is to conduct a randomized prospective clinical trial to determine whether no antibiotics in OHCA patients in the ED with very low likelihood of infection is non-inferior to early antibiotic treatment. Hypothesis a: 28-day all-cause mortality will be non-inferior in OHCA patients with very low likelihood of infection who do not receive antibiotic therapy compared with those who receive early antibiotic therapy Hypothesis b: There will be no difference in subsequent incidence of proven infections in the no antibiotics vs, early antibiotics groups Hypothesis c: There will be no difference in the length of ICU stay and overall hospital stay in the early antibiotics vs. no antibiotics groups

Condition or Disease Intervention/Treatment Phase
  • Other: No use of antibiotics
  • Other: with antibiotics treatment
N/A

Detailed Description

As above

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1000 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Impact of Early Antibiotics on Non-Traumatic Out of Hospital Cardiac Arrest (OHCA)
Actual Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Subject with antibiotics treatment

Individuals with low risk of infection after OHCA will be randomized to either 1) early antibiotics, or 2) no antibiotics. Experimental arm received antibiotics as per local hospital clinical care pathways and physician choice.

Other: with antibiotics treatment
with antibiotics treatment

Active Comparator: Subjects with no antibiotics treatment

Individuals with low risk of infection after OHCA will be randomized to either 1) early antibiotics, or 2) no antibiotics. Active comparator arm will receive no antibiotics,

Other: No use of antibiotics
Subjects will be randomized into antibiotics and no antibiotics groups based on inclusion and exclusion criteria

Outcome Measures

Primary Outcome Measures

  1. 28-day all-cause mortality. likelihood of infection whether they receive early antibiotic therapy or not. [28-day]

    Primary outcome measure is 28-day all-cause mortality in persons who receive no antibiotics compared with those who receive early antibiotics in OHCA patients.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ● Adults aged >18 years, presenting to HGH ED after out-of-hospital cardiac arrest

  • Patients with low likelihood of infection as per the definitions provided above

  • Ability to obtain informed consent from the subjects or their next of kin/family member/legal surrogate in case of incapacitation due to sedation, mechanical ventilation, etc. In case the next of kin is not available, an independent physician who is not a part of the investigative team will complete and sign the checklist as per HMC Policy "RES 11026_Appendix 6.5". (see section 4.1.3 for details) A member of the investigative team and a witness will also sign this form before the potential subject is enrolled in the study.

Exclusion Criteria:
  • Patients who have clear evidence of infection, as defined by criteria for the study.

  • Patients who have received antibiotics within the last 1 week prior to admission.

  • Patients with malignancy, except those who have been cured or in complete remission.

  • Females with known pregnancy.

  • Known immunocompromised states (including HIV/AIDS, transplant recipients on immunosuppressant drugs, long-term [> 3 weeks of prednisone >5mg/day equivalent] steroid therapy).

  • Patients on immunologic disease modifying agents (commonly known as "biologics")

  • Patients considered "brain-dead" or "vegetative state"

  • Patients transferred from another hospital, long term care facility or institution

  • Neutropenia (total WBC <1,500/mm3 or absolute neutrophil count of <1,000/mm3)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hamad Medical Corporation Doha Qatar

Sponsors and Collaborators

  • Hamad Medical Corporation

Investigators

  • Principal Investigator: Adeel A Butt, MBBS, MS, Hamad Medical Corporation

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Adeel Ajwad Butt, Senior Consultant in Infectious Diseases, Hamad Medical Corporation
ClinicalTrials.gov Identifier:
NCT05914779
Other Study ID Numbers:
  • IRGC-05-SI-18-356
First Posted:
Jun 22, 2023
Last Update Posted:
Jun 22, 2023
Last Verified:
Jun 1, 2023
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 Jun 22, 2023