Clinical Trial

Predictors of Transmural Non-Occlusive Mesenteric Ischemia in ICU Patients With Suspected Acute Mesenteric Ischemia

Study acronym: AMESI-EST
Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated May 28, 2026 (before its estimated June 5, 2026 completion). Its status may not reflect the trial's current state.
Summary
Acute mesenteric ischemia (AMI) is a rare but life-threatening condition associated with high mortality and major diagnostic challenges due to nonspecific clinical presentation and limited reliable biomarkers. Critically ill patients in the intensive care unit (ICU) are at particularly high risk of non-occlusive mesenteric ischemia (NOMI), a subtype of AMI characterized by impaired mesenteric perfusion without large-vessel occlusion. Despite advances in imaging, the diagnosis of NOMI remains difficult, and data specifically focusing on ICU patients with suspected AMI are limited. This prospective observational multicenter study aims to identify independent predictors of transmural NOMI among ICU patients with suspected AMI. In addition, the study will describe demographics, comorbidities, clinical presentation, laboratory findings, diagnostic imaging, management strategies, and outcomes among ICU patients with NOMI, other forms of AMI, and patients with suspected but unconfirmed AMI. Consecutive adult ICU patients in whom clinical suspicion of AMI arises during ICU stay will be included across Estonian regional hospitals. The study is a local continuation of the international AMESI study, with a specific focus on critically ill ICU patients.
Trial Details
NCT Number NCT07610356
Lead Sponsor University of Tartu
Conditions Non-Occlusive Mesenteric Ischaemia (NOMI), Acute Mesenteric Ischemia
Enrollment 150 participants
Start Date 2022-06-06
Primary Completion 2026-06-05 (estimated)
Study Completion 2026-09-05 (estimated)
Updated on ClinicalTrials.gov 2026-05-28