Measuring a biomarker in patients with chronic mesenteric ischemia
Official title: Intestinal Ischemia Biomarker and Quality of Life of the Patients With Chronic Mesenteric Ischemia and Median Arcuate Ligament Syndrome
Run by Oslo University Hospital · NCT06468774 · Data updated 2026-11-12
This study is testing if measuring a specific protein in the blood can help doctors better understand and treat patients with chronic mesenteric ischemia and related conditions.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 180 (estimated) |
| Sponsor | Oslo University Hospital Academic / other |
| Locations | 1 site (Oslo, Oslo) |
| Status | Recruiting |
| Started | June 10, 2024 |
| Main results expected | May 31, 2037 |
| Study ends | May 31, 2037 |
| Registry record updated | July 30, 2025 |
| Trial ID | NCT06468774 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 years with a diagnosis of CMI or MALS who are scheduled for surgical intervention.
✕Probably not a fit
Patients under 18 years or those who have not provided informed consent will not benefit from this study.
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 aims to compare plasma levels of Alpha glutathione S transferase (Alpha GST) in patients diagnosed with chronic mesenteric ischemia (CMI) and median arcuate ligament syndrome (MALS) against individuals with Morbus Crohn, gallstone disease, and healthy controls. The study will include patients scheduled for surgical treatment and will assess changes in Alpha GST levels pre- and post-treatment. Additionally, it will evaluate the health-related quality of life of participants. The goal is to identify a reliable biomarker for intestinal ischemia that could aid in diagnosis and treatment decisions.
Why it matters
Potential benefit: If successful, this study could lead to a reliable biomarker for diagnosing chronic mesenteric ischemia and median arcuate ligament syndrome, improving patient outcomes.
How similar studies have gone: Previous studies have indicated raised levels of Alpha GST in patients with CMI and MALS, but this study aims to provide a more robust comparison with control groups.
Who can join: the full rules
Show full inclusion / exclusion criteria
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. \-
Where it's running
-
Department of vascular surgery, Oslo University Hospital
Oslo, Oslo, Norway Recruiting
Study contacts
- Principal investigator: Syed Sajid Hussain Kazmi, MD, PhD — Department of vascular surgery, Oslo University Hospital
- Study coordinator: Syed Sajid Hussain Kazmi, MD, PhD
- Email: sshkazmi@gmail.com
- Phone: 4792468309
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.