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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04662268
Other study ID # RECHMPL20_0639
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2014
Est. completion date November 30, 2020

Study information

Verified date December 2020
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our objective is to determine a prognostic score including CT, clinical and biological criteria predicting the serious (death / surgery) or non-serious (medical treatment) evolution of ischemic colitis and therefore possibly modify the therapeutic management (propose surgical treatment for a severe form based on prognostic score).


Recruitment information / eligibility

Status Completed
Enrollment 206
Est. completion date November 30, 2020
Est. primary completion date November 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Age > or = at 18 years old; - Performing an abdomino-pelvic scan injected within 6 hours of the onset of symptoms; - Ischemic colitis proven by endoscopy or surgical data. Exclusion criteria: - CT scan performed without injection and / or after 6 hours following the onset of symptoms; - Unproven ischemic colitis.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complication rate of ischemic colitis Severe (surgery and/or death) or non severe form of ischemic colitis (medical treatment) : analysis of radiological, biological and clinical data is performed at the time of acute episode of ischemic colitis when the patient is admitted to the hospital or during the stay of the patient previously present in the hospital for another condition 1 day