Evaluating CT imaging for identifying treatable bowel in acute mesenteric ischemia
The Feasibility of a Radiological Score Based on Quantified Analysis of Computed Tomography Signs for Recognizing Salvageable Bowel in Acute Mesenteric Ischemia: A Retrospective Analysis of Prospective Study
This study is testing a new way to use CT scans to help doctors find parts of the bowel that can still be saved in patients with acute mesenteric ischemia.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Tartu Academic / other |
| Locations | 1 site (Tartu) |
| Trial ID | NCT06445660 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of a radiological scoring system based on CT signs to identify salvageable bowel in patients with acute mesenteric ischemia (AMI). By analyzing CT scans, the study aims to differentiate between reversible and irreversible ischemic damage, which is crucial for determining appropriate treatment strategies. The research is part of a larger observational study focused on the incidence and outcomes of AMI in hospitalized adults. The goal is to enhance diagnostic performance and potentially improve patient outcomes by preserving intestinal viability through timely intervention.
Who should consider this trial
Good fit: Ideal candidates are adults participating in the AMESI study who have confirmed or suspected acute mesenteric ischemia and have undergone a CT scan with intravenous contrast.
Not a fit: Patients who have not undergone a full abdominal CT scan with intravenous contrast or those with scans that do not meet the study criteria may not benefit.
Why it matters
Potential benefit: If successful, this approach could lead to better treatment decisions and improved preservation of bowel function in patients with acute mesenteric ischemia.
How similar studies have performed: While this study builds on existing knowledge of CT imaging in AMI, the specific scoring system being tested is novel and has not been widely validated in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participant in AMESI study * confirmed or suspected acute mesenteric ischaemia * CT scan of the entire abdominal cavity / full body using intravenous contrast media is available Exclusion Criteria: * Scans without the use of an intravenous contrast media or those covering only a partial area of the abdomen will be excluded.
Where this trial is running
Tartu
- Tartu University Hospital — Tartu, Estonia (Recruiting)
Study contacts
- Study coordinator: Joel Starkopf
- Email: joel.starkopf@ut.ee
- Phone: 53318400
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.