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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06212921
Other study ID # BIPAMI study
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 2024
Est. completion date September 2025

Study information

Verified date January 2024
Source University of Tartu
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 250
Est. completion date September 2025
Est. primary completion date September 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Sequential blood samples
Sequential blood samples for diagnostic tests is the only intervention in thei study

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Tartu

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of correctly predicted cases of acute mesenteric ischaemia Rate of correctly predicted cases of Acute mesenteric ischaemia using different biomarkers 10 months
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