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Demographics, Diagnosis, Management, and Outcomes of Non-occlusive Mesenteric Ischemia.

Demographics, Diagnosis, Management, and Outcomes of Non-occlusive Mesenteric Ischemia: a Substudy of a Prospective Multicenter Observational Study (AMESI)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06970015
Enrollment
566
Registered
2025-05-14
Start date
2022-06-06
Completion date
2025-12-31
Last updated
2025-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-Occlusive Mesenteric Ischemia

Brief summary

This prospective multicenter observational study, conducted between June , 2022, and April, 2023, is a preplanned analysis of the AMESI study titled 'Demographics, diagnosis, management, and outcomes of non-occlusive mesenteric ischemia,' aiming primarily to describe the demographic profile, clinical presentation, and laboratory findings of patients with non-occlusive mesenteric ischemia (NOMI), and secondarily to identify independent risk factors as well as diagnostic approaches, management strategies, and outcomes-including in-hospital, 90-day, and one-year results.

Interventions

OTHERNo intervention

No intervention, this is an observational study on patients with suspected acute mesenteric ischemia

Sponsors

University of Tartu
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

All at least 18-year-old patients with acute mesenteric ischemia or patients suspected of acute mesenteric ischemia that was not confirmed * Patients with arterial occlusive AMI * Patients with non-occlusive mesenteric ischemia * Patients with venous occlusive AMI * Patients with unclear mechanism of AMI * Patients with suspected but not confirmed AMI

Exclusion criteria

* Patients with other specific form of AMI (e.g dissection) * Confirmed strangulating bowel obstruction * Individuals under 18 years of age. * Consent declined by patient or next of kin * Chronic mesenteric ischaemia without an acute event

Design outcomes

Primary

MeasureTime frameDescription
Arterial Blood pH in Patients with Non-Occlusive Mesenteric IschemiaBaselineArterial pH level. Normal range is 7.35-7.45. Lower values indicate acidosis.
Demographic profileBaselineOne of the primary objectives is to describe the baseline demographic profile of patients with non-occlusive mesenteric ischemia. The demographic data will include the following information: 1. Gender (Male or Female) 2. Age (in years) 3. BMI (calculated from body weight in kilograms and height in centimeters)
SOFA scoreBaselineSequential Organ Failure Assessment (SOFA) score. Range: 0-24. Higher scores indicate more severe organ dysfunction.
Serum Lactate Levels in Patients with Non-Occlusive Mesenteric IschemiaBaselineSerum lactate level measured in mmol/L. Higher values indicate worse tissue perfusion.
Baseline APACHE II ScoreBaselineAcute Physiology and Chronic Health Evaluation II (APACHE II) score. Range: 0-71. Higher scores indicate more severe disease and higher predicted mortality.

Secondary

MeasureTime frameDescription
ManagementBaselineRate of surgical, conservative, endovascular or palliative management
30-day survival30 days after admission30-day Survival of patients with non-occlusive mesenteric ischemia
1-year survival1 year1-year survival of patients with non-occlusive mesenteric ischemia
Rate of Patients Diagnosed with Non-Occlusive Mesenteric Ischemia by CT, Endoscopy, or AngiographyBaselinePercentage of participants diagnosed with non-occlusive mesenteric ischemia (NOMI) using computed tomography (CT), endoscopy, or angiography.

Countries

Estonia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026