Not medical advice. Talk to your doctor and the trial team before making any decision about a clinical trial.
PSC Trial Watch
Crohn'sRecruiting

Intestinal Ischemia Biomarker in Patients With Chronic Mesenteric Ischemia

Observational · No treatment assigned · 1 site · Oslo University Hospital

Official record & contacts on ClinicalTrials.gov ↗

In plain English

What this trial is testing

Condition(s) listed: Chronic Mesenteric Ischemia, Median Arcuate Ligament Syndrome and Crohn Disease. This is an observational study: researchers collect information (for example questionnaires, samples, or scans) but the study does not assign a treatment.

Who can join

Some of the main requirements, copied from the record:

Plus 4 more requirement(s). Only the trial team can confirm whether you qualify.

What's involved

Main thing being measured

In the researchers’ words

Plasma Alpha glutathione S transferase (Alpha GST) has been previously demonstrated to be raised in patients with chronic mesenteric ischemia (CMI) caused by atherosclerosis and in patients with median arcuate ligament syndrome (MALS). Raised plasma level of Alpha GST has been demonstrated to decrease or normalize after surgical treatment of patients with CMI and MALS as compared with healthy individuals.

This is a short automatic summary built from the official record. A fuller plain-English card is coming; until then, please read the official record.

Questions to ask your doctor and the trial team

Official details

StatusRecruiting
PhaseObservational
Study typeObservational
ConditionsChronic Mesenteric Ischemia; Median Arcuate Ligament Syndrome; Crohn Disease; Cholelithiasis
Lead sponsorOslo University Hospital
Enrollment180 (estimated)
Start date2024-06-10
Primary completion (est.)2037-05-31
First posted2024-06-21
Last updated2025-07-30
Official titleIntestinal Ischemia Biomarker and Quality of Life of the Patients With Chronic Mesenteric Ischemia and Median Arcuate Ligament Syndrome
ClinicalTrials.gov IDNCT06468774

Interventions

Full eligibility criteria (from the record)
Inclusion Criteria: Above 18 years and has given informed written consent for treatment and study participation

For the patient groups :

Group 1: Has CTA or ultrasound diagnosed MALS and is scheduled operative treatment.

Group 2: Has CTA or ultrasound diagnosed CMI and is scheduled operative or endovascular treatment.

For the control group:

Group 3- Has ultrasound based diagnosis of cholelithiasis and is scheduled for cholecystectomy.

Group 4- Has established Mb Crohn diagnosis and under gastric lab follow-up. Group 5- Young healthy blood donors of mean age 45 years and has excluded MALS or CMi with ultrasound.

Group 6- Healthy blood donors of mean age 70 years and has excluded MALS or CMi with ultrasound.

Exclusion Criteria: Age less than 18 years Has nor given written consent.

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Locations (1)

SiteCityCountrySite status
Department of vascular surgery, Oslo University HospitalOslo, OsloNorwayRecruiting

For contacts at each site, use the official record.

Information only, not medical advice. Talk to your doctor and the trial team before making any decision about a clinical trial.