Ignite Creation Date:
2024-06-16 @ 11:50 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06445660
Status:
RECRUITING
Last Update Posted:
2024-06-06
First Post:
2024-05-22
Brief Title:
The Feasibility of a Radiological Score Based on CT Signs for Recognizing Salvageable Bowel in Acute Mesenteric Ischemia
Sponsor:
University of Tartu
Organization:
University of Tartu
Study Overview
Official Title:
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
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
AMESIradiol
Brief Summary:
Computed tomography CT is the standard modality for scanning patients with critical acute abdominal conditions including suspected acute mesenteric ischemia AMI CT imaging can potentially differentiate between reversible and irreversible ischaemic damage of the bowel This moment is pivotal in selecting the treatment strategy for AMI - in the absence of irreversible damage reperfusion therapy can preserve intestinal viability thereby avoiding the need for bowel resection The present study tests the hypothesis that combining several symptoms may enhance the diagnostic performance of CT scanning in detecting salvageable bowel in patients with AMI This study is an ancillary component of the AMESI study Clinical Trials NCT05218863 - a prospective multicentre observational study aimed at identifying the incidence and describing the outcomes of acute mesenteric ischemia AMI in adult hospitalized patients The ultimate purpose of the present study is to create a computed tomography-based radiological score for the assessment of bowel viability in patients with AMI
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None