Identifying biomarkers for acute intestinal ischemia
Searching Biomarkers of Acute Intestinal Ischemic Injuries
This study is trying to find new markers in the blood that can help doctors quickly diagnose acute intestinal ischemia in patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 556 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Clichy) |
| Trial ID | NCT03518099 on ClinicalTrials.gov |
What this trial studies
This study aims to identify accurate biomarkers for acute mesenteric ischemia, particularly in its early stages. It involves analyzing biological samples from patients and controls, which will be stored in a biological library for further examination. The analysis will be conducted at several prestigious institutions, including Paris V University and Imperial College London, using both established and novel -omics methods to determine candidate markers. The goal is to improve diagnostic capabilities and treatment strategies for this severe condition.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old who present with acute abdominal pain and require a CT scan for diagnosis.
Not a fit: Patients who do not undergo an abdominal CT scan or are under 18 years old may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to earlier and more accurate diagnosis of acute mesenteric ischemia, potentially reducing mortality rates and improving patient outcomes.
How similar studies have performed: Other studies have shown promise in identifying biomarkers for similar conditions, but this specific approach is innovative and may provide new insights.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Clichy
- Corcos Olivier — Clichy, France (Recruiting)
Study contacts
- Study coordinator: olivier corcos
- Email: olivier.corcos@aphp.fr
- Phone: 140875000
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.