Intestinal Vascular Emergency Unit for Mesenteric Ischemia

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on the management of mesenteric ischemias, including both acute and chronic forms, as well as intestinal vascular diseases without ischemia. The study is conducted at the first dedicated Intestinal Vascular Emergency Unit in Paris, which combines advanced resuscitation techniques, interventional radiology, and specialized knowledge to improve patient outcomes. The unit has significantly increased survival rates for acute mesenteric ischemia while reducing the need for intestinal resections. The study aims to gather data on patient outcomes and the effectiveness of this specialized care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age \> 18 years old
* IMVI including :
* acute mesenteric ischaemia defined by acute digestive distress in relation to arterial and/or venous, occlusive and/or non-occlusive splanchnic-mesenteric vascular insufficiency, in the absence of an alternative diagnosis

  * Chronic mesenteric ischaemia defined by chronic digestive distress (duration of symptom evolution \>30 days) related to occlusive or non- occlusive arterial or venous vascular insufficiency.
  * MVI: gastrointestinal arterial or venous diseases without ischaemia (atheroma, embolism, thrombosis, dissection, mediolysis, aneurysm, dysplasia, sheathing, compression, torsion)

Exclusion Criteria:

* Left ischaemic colitis without damage to the celiac trunk and/or superior mesenteric artery
* Dissection of the abdominal aorta without intestinal ischaemia
* Portal thrombosis without extension to the superior mesenteric vein
* Portal thrombosis without extension to the superior mesenteric vein
* Traumatic rupture of the digestive arteries
* Non-injected abdominal scanner or no abdominal scanner
* Patient opposition to participation in research
* Patient under guardianship / curators
* Vulnerable patient: pregnant or breastfeeding women, persons deprived of their liberty, minors, adults unable or unwilling to give consent

Where it's running

• Olivier CORCOS
  Clichy, France Recruiting

Study contacts

• Study coordinator: Olivier CORCOS
• Email: olivier.corcos@aphp.fr
• Phone: 0140875000

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.