NCT06212921RecruitingNot Applicable
Biomarkers In Prediction of Acute Mesenteric Ischaemia: a Prospective Multicentre Study (BIPAMI Study)
University of Tartu4 sites in 2 countries250 target enrollmentStarted: October 14, 2024Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- University of Tartu
- Enrollment
- 250
- Locations
- 4
- Primary Endpoint
- Rate of correctly predicted cases of acute mesenteric ischaemia
Study Overview
Brief Summary
Current study will be undertaken to identify combinations of biomarkers that can reliably identify acute mesenteric ischaemia (AMI) and distinguish between non-transmural and transmural ischaemia. Different combinations of biomarkers for different sub-types and severity of AMI, and different time points of measurement after onset of symptoms.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Diagnostic
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Age 18 years or older
- •Initial decision in favour of further diagnostics of mesenteric ischaemia
Exclusion Criteria
- •Age <18 years
- •Consent declined by patient or next of kin (delayed consent)
- •Chronic mesenteric ischaemia without an acute event
- •Immediate decision for withdrawal of further diagnostics and active treatment
- •Referral from another hospital with already established diagnosis of AMI
- •AMI diagnosed at surgery without previously having been considered
Outcomes
Primary Outcomes
Rate of correctly predicted cases of acute mesenteric ischaemia
Time Frame: 10 months
Rate of correctly predicted cases of Acute mesenteric ischaemia using different biomarkers
Secondary Outcomes
No secondary outcomes reported
Investigators
Annika Reintam Blaser
Associate Professor
University of Tartu
Study Sites (4)
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