Incidence of Colon Ischemia in Patients After Cardiopulmonary Resuscitation (CPR)
1 other identifier
interventional
200
1 country
1
Brief Summary
Bedside colonoscopy 24-36 hours after successful CPR
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 19, 2025
CompletedStudy Start
First participant enrolled
January 7, 2026
CompletedFirst Posted
Study publicly available on registry
January 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 6, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 6, 2028
January 22, 2026
January 1, 2026
2 years
December 19, 2025
January 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Detection of colon ischemia
Detection of colon ischemia within 30 days after return of spontaneous circulation
from baseline (0 hours) until day 30
Secondary Outcomes (10)
in-hospital mortality
from baseline (0 hours) until hospital discharge
abdominal surgery ((hemi-)colectomy)
from baseline (0 hours) until hospital discharge
functional outcome
day 30, day 60 and day 90
Liver function
within 0-72 hours after CPR
renal function
within 0-72 hours after CPR
- +5 more secondary outcomes
Study Arms (1)
early colonoscopy after successful CPR
OTHERbedside colonoscopy 24-36 hours after successful CPR
Interventions
bedside colonoscopy without bowel cleansing early (24-36h) after successful CPR
Eligibility Criteria
You may qualify if:
- adult patients (≥ 18 years) admitted to the participating department AND
- in-hospital or out-of-hospital cardiac arrest (IHCA, OHCA)
You may not qualify if:
- resuscitation period of ≤ 5 minutes
- awake and contactable patients (GCS ≥ 13)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medical Center - University of Freiburg
Freiburg im Breisgau, 79106, Germany
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Physician
Study Record Dates
First Submitted
December 19, 2025
First Posted
January 22, 2026
Study Start
January 7, 2026
Primary Completion (Estimated)
January 6, 2028
Study Completion (Estimated)
February 6, 2028
Last Updated
January 22, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share