Assessment of Quality of Life After Acute Mesenteric Ischemia
EQVIMA-1
1 other identifier
observational
100
1 country
1
Brief Summary
Acute mesenteric ischemia is a severe abdominal emergency associated with a poor prognosis. While numerous studies have been conducted on the incidence, outcomes, and risk factors of mesenteric ischemia, very few focus on the quality of life of patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 24, 2024
CompletedFirst Submitted
Initial submission to the registry
December 11, 2025
CompletedFirst Posted
Study publicly available on registry
December 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedDecember 24, 2025
December 1, 2025
1.4 years
December 11, 2025
December 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Score of GIQLI (Gastrointestinal Quality of Life Index)
The GIQLI quality of life score consists of 36 items: the higher the score, the better the quality of life.
Up to 12 months
Eligibility Criteria
Adult patient (≥ 18 years) treated for mesenteric ischemia in the Strasbourg University Hospitals
You may qualify if:
- Adult patient (≥ 18 years)
- Treated for mesenteric ischemia between 2010 and 2022 in the intensive care, cardiovascular, and digestive and vascular surgery departments of the Strasbourg University Hospitals
You may not qualify if:
- Chronic mesenteric ischemia or other non-ischemic intestinal vascular pathologies such as mechanical causes.
- Colonic ischemia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service d'Anesthésie - CHU de Strasbourg - France
Strasbourg, 67091, France
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 11, 2025
First Posted
December 24, 2025
Study Start
October 24, 2024
Primary Completion
April 1, 2026
Study Completion
April 1, 2026
Last Updated
December 24, 2025
Record last verified: 2025-12