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Clinical Trials in France / NCT03518099
Recruiting Not applicable

Searching Biomarkers of Acute Intestinal Ischemic Injuries

NCT03518099 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2018-11-16
Last updated
2025-12-16

Condition(s) studied

Acute Mesenteric Ischemia

Investigational drug(s) / intervention(s)

blood sampling →

blood sampling: Two tubes of 5ml of blood will be collected for Serum collection, 3 tubes of 5 ml of blood taken for plasma collection and 2 tubes of 7 ml of blood taken for DNA collection

Study summary

The aim of the SURVIBIO study is to characterize accurate biomarkers for acute mesenteric ischemia, in particular at early stages.

In the study, the development of biomarkers will be based on the analysis of human biological samples from patients and controls that will be conserved in a biological library. Samples will be analysed in the Laboratory for Vascular Translational Sciences (LVTS, Inserm U1148), in the Department of Biochemistry (Pr Puy, Dr Peoc'h), in Paris V university , in Imperial College of London (Pr Dumas), in Jacques Monod Institute and in Maastricht University Medical Center . The candidate markers will be determined according to an a priori method (form markers already described in the literature) and with no a priori strategy using -omics methods.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * age\> 18 years * Acute abdominal pain requiring an injected abdominal injected CT scan, at best at non-injected / early arterial / portal time * Admitted or attended in Beaujon and / or Bichat hospitals * Patient covered by a social security scheme * Written consent Exclusion Criteria: • lack of abdominal CT scan

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Corcos Olivier Clichy France Recruiting

More Assistance Publique - Hôpitaux de Paris trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03518099 on ClinicalTrials.gov ↗ ← All trials in France