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Mesenteric Ischemia Markers Study In The Presence Of Mesenteric Arteries Disease

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• 18 years or older, all sex

• Initial decision, the presence of angio-visualisation of the MA and suspicion of mesenteric arteries diseases

• Patient's consent to participate in the study

• No pregnancy, no history of major operations on MA, the gastrointestinal tract and digestive organs (except appendectomy, endoscopic polypectomy).

Locations
Other Locations
Belarus
Belarusian State Medical University
RECRUITING
Minsk
Contact Information
Primary
Hleb But-Husaim, PhD
dr.buthusaim@gmail.com
+375256139407
Time Frame
Start Date: 2025-12-22
Estimated Completion Date: 2026-12-12
Participants
Target number of participants: 120
Treatments
Other: MA data and blood samples data
Patients with MA lesions and suspicion of acute or chronic vascular diseases of the intestine. Patients with suspicion of AMI or CMI are to be included and blood samples are to be collected. Blood samples is the only intervention.
Related Therapeutic Areas
Sponsors
Leads: Belarusian State Medical University

This content was sourced from clinicaltrials.gov