Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07460700

Mesenteric Ischemia Markers Study

Led by Belarusian State Medical University · Updated on 2026-03-10

120

Participants Needed

1

Research Sites

50 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Vascular bowel disease remains a socially significant and potentially fatal condition (if it develops into AMI), primarily due to delayed diagnosis. Blood biomarkers are theoretically ideal for early risk stratification (like troponins in myocardial infarction). However, the existing evidence base is characterized by low quality and high heterogeneity, which hinders their use in clinical practice. Therefore, there is an urgent and unmet clinical need for high-quality, methodologically rigorous research to validate biomarkers in MI. A current study (MESMARK) is to be undertaken to identify combinations of biomarkers that can reliably identify mesenteric ischemia (MI) and distinguish between non-transmural and transmural clinical relevant ischemia.

CONDITIONS

Official Title

Mesenteric Ischemia Markers Study

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older, all sexes
  • Presence of angio-visualization of mesenteric arteries and suspicion of mesenteric artery disease
  • Patient consents to participate in the study
  • No pregnancy
  • No history of major surgeries on mesenteric arteries, gastrointestinal tract, or digestive organs (except appendectomy or endoscopic polypectomy)
Not Eligible

You will not qualify if you...

  • Patient or relatives decline consent
  • Failure to meet inclusion criteria

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Belarusian State Medical University

Minsk, Belarus

Actively Recruiting

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Research Team

H

Hleb But-Husaim, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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