Verbetering in de diagnostiek van een doorbloedingsstoornis van de darm
Recruiting
- Conditions
- Acute Intestinal Ischemia
- Registration Number
- NL-OMON22199
- Lead Sponsor
- Academisch ziekenhuis Maastricht (azM)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
Age = 18 years
All consecutive patients admitted to one of the participating medical centers emergency departments (ED) or at the intensive care unit (ICU) with clinical suspicion of acute intestinal ischemia, which is based on;
oclinical manifestation;
ophysical examination by the physician;
olaboratory measurements;
ophysician’s consideration to perform computed tomography (CT)-scan
Exclusion Criteria
Age = 18 years
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint of the study is the early and accurate identification of presence and severity of acute intestinal ischemia in patients. The main study parameters are plasma biomarkers indicative for intestinal damage of patients suspected of acute intestinal ischemia.
- Secondary Outcome Measures
Name Time Method Detection of volatile organic compounds (VOC) in exhaled air of patients suspected of acute intestinal ischemia.