Clinical Trials in Norway / NCT02914912
Active, not recruiting
Observational
Investigation of Chronic Intestinal Ischemia
NCT02914912 · tracked via the Priya Life Science Norway tracker
Condition(s) studied
Chronic Mesenteric Ischemia
Study summary
Patients suspected of chronic mesenteric ischemia caused by atherosclerosis or median arcuate ligament syndrome shall be investigated with trans mucosal and transserosal laser Doppler flowmeter and visible light spectroscopy.
Eligibility
Inclusion Criteria:
Clinical chronic mesenteric ischemia caused by either atherosclerosis or median arcuate ligament syndrome
Exclusion Criteria:
Patients unable to go through gastroscopy
Primary outcome measure(s)
- Transmucosal Oxygen concentration of the stomach and duodenum — Baseline, 3 months and 12 months
Repeated measurments at baseline 3, and 12 months after the surgical or endovascular treatment of chronic mesenteric ischemia (CMI) and median arcuate ligament syndrome (MALS) shall be performed. With the help of gastoscopy assisted Laser Doppler flowmeter and visible light spectroscopy, transmocosal SaO2, rHb concentration, flow and velocity in arbitrary units shall be measured.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Oslo University Hospital | Oslo | Norway | |
| Department of vascular surgery, Oslo University Hospital | Oslo | Norway |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT02914912 on ClinicalTrials.gov ↗ ← All trials in Norway