Under construction – not a live service
Sign in
Taking people in NorwayNo phase

Blood Marker and Quality of Life in Chronic Intestinal Blood Flow Problems

Compares a blood marker in adults with chronic bowel blood flow problems to other people.

Plain-language title generated from the registry record
Registry title: Intestinal Ischemia Biomarker in Patients With Chronic Mesenteric Ischemia

Key facts

Where
Oslo, NorwaySee the site

Where in Norway

  • Department of vascular surgery, Oslo University HospitalOslo, NorwayTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Oslo University Hospital
Trial code
NCT06468774
Record updated
30 July 2025
Original description
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.Read full original descriptionShow less

Intestinal Ischemia Biomarker and Quality of Life of the Patients With Chronic Mesenteric Ischemia and Median Arcuate Ligament Syndrome

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 study compares the plasma Alpha GST in patients with CMI and MALS with those with 1-Morbus Crohn, 2-Gallstone disease, and age-matched healthy individuals.

Besides, changes in the health-related quality of life (QoL) will be investigated in the study individuals.

Inclusion: 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: -.

ClinicalTrials.gov NCT06468774