Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:46 PM
Ignite Modification Date:
2025-12-24 @ 10:46 PM
NCT ID:
NCT07182669
Eligibility Criteria:
Inclusion Criteria:
* \- Written informed consent
* Male or female persons \> 18 years
* Subjects with postprandial abdominal pain considered compatible with mesenteric ischemia, and severe stenosis of the SMA and eventually other mesenteric arteries, diagnosed with CT-angiography or Doppler ultrasound
* OR subjects with severe stenosis of the SMA and eventually other mesenteric arteries, diagnosed with CT-angiography or Doppler ultrasound, but not postprandial pain
Exclusion Criteria:
* \- Serious concurrent illness
* BMI \> 30
* Cardiac arrhythmia
* Anemia with Hgb \< 7,0 mmol/l
* Pregnancy or breastfeeding (urine HCG is performed on all fertile women)
* Systolic blood pressure \< 90 or \> 200 mmHg
* Claustrophobia
* Patients who, in the judgement of the investigator, is incapable of participating
* Metallic foreign objects in the body, or pacemakers
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07182669
Study Brief:
Protocol Section:
NCT07182669