Actively Recruiting

Age: 18Years +
All Genders
ID04746534

Cohort SURVI: Observational Study of Intestinal Ischemia and Vascular Diseases

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2021-02-09

20000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating intestinal ischemia and related vascular diseases through a specialized intensive care unit called SURVI, established within the Paris-Nord Val de Seine University Hospital Group with support from AP-HP. This unit focuses on managing acute and chronic mesenteric ischemias and intestinal vascular diseases without ischemia. These conditions involve serious blood flow problems in the digestive system, and without treatment, acute mesenteric ischemia can be fatal. The study aims to better understand the prevalence, risks, and outcomes of these rare and varied vascular diseases over time. This research is an observational study that follows a group of patients with intestinal vascular ischemia (IMVI) and other intestinal vascular diseases without ischemia (IIVD). Patients included have conditions such as acute or chronic mesenteric ischemia or other arterial or venous gastrointestinal vascular diseases. The study collects data to track the natural history of these diseases, as current knowledge about their progression and outcomes is limited. No experimental treatments are administered; instead, patient health and disease progression are monitored over the years. Participants in this study will be followed longitudinally with assessments focused on mortality rates at one and five years, disease prevalence, risk factors for complications like intestinal resection, and rates of vascular restenosis or ischemic events. The study also examines the impact of these diseases on outcomes such as short intestinal syndrome and dependence on parenteral nutrition after surgery. Data collection includes clinical evaluations and medical records over an extended period, allowing researchers to better understand disease patterns and factors affecting patient survival and quality of life.

CONDITIONS

Brief Title

Cohort SURVI : Intestinal Ischemia and Vascular Diseases

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years old
  • Diagnosis of acute mesenteric ischemia defined by acute digestive distress with arterial and/or venous, occlusive and/or non-occlusive splanchnic-mesenteric vascular insufficiency without an alternative diagnosis
  • Diagnosis of chronic mesenteric ischemia defined by chronic digestive distress lasting more than 30 days related to occlusive or non-occlusive arterial or venous vascular insufficiency
  • Gastrointestinal arterial or venous diseases without ischemia such as atheroma, embolism, thrombosis, dissection, mediolysis, aneurysm, dysplasia, sheathing, compression, or torsion
Not Eligible

You will not qualify if you...

  • Left ischemic colitis without damage to the celiac trunk and/or superior mesenteric artery
  • Dissection of the abdominal aorta without intestinal ischemia
  • Portal thrombosis without extension to the superior mesenteric vein
  • Traumatic rupture of the digestive arteries
  • No abdominal scanner performed or non-contrast abdominal scanner
  • Patient opposes participation in research
  • Patient under guardianship or curatorship
  • Vulnerable patients including pregnant or breastfeeding women, persons deprived of their liberty, minors, or adults unable or unwilling to give consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 5 years

Participants who have intestinal ischemia and vascular diseases are observed over time to study disease progression, complications, and mortality.

Periodic visits over 5 years

Trial Site Locations

Total: 1 location

1

Olivier CORCOS

Clichy, France, 92110

Actively Recruiting

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Research Team

O

Olivier CORCOS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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