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Endoscopic Relapse Risks Evaluation After Ileocolic Resection for Crohn's Disease - Trial NCT06299631

Access comprehensive clinical trial information for NCT06299631 through Pure Global AI's free database. This phase not specified trial is sponsored by University Hospital, Montpellier and is currently Completed. The study focuses on Crohn's Disease. Target enrollment is 133 participants.

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NCT06299631
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Trial Details
ClinicalTrials.gov โ€ข NCT06299631
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Endoscopic Relapse Risks Evaluation After Ileocolic Resection for Crohn's Disease
Endoscopic Relapse Risk Factors After Ileocolic Resection on Crohn's Disease Patients in the Biologic Era

Study Focus

Crohn's Disease

Ileocolic resection

Observational

procedure

Sponsor & Location

University Hospital, Montpellier

Montpellier, France

Timeline & Enrollment

N/A

Jan 01, 2015

Dec 01, 2023

133 participants

Primary Outcome

Endoscopic recurrence rate

Summary

Aim of the study:
 
 To evaluate risk factors of endoscopic relapse after ileocolic resection in a cohort of
 Crohn's disease patients treated with anti-TNF agents.
 
 Methods:
 
 From 2014 to 2022, all consecutive patients who underwent ileocolic resection for Crohn's
 disease treated with anti-TNF agents in two referral tertiary center were prospectively
 collected.
 
 Considering exclusion criteria, data from 114 patients were analyzed. The cohort was
 separated into 2 groups according to study period.
 
 Short and long-term outcomes were compared between the two groups.
 
 Primary outcome:
 
 Endoscopic recurrence (defined as i2 lesions according to Rutgeerts classification) 6
 months after surgery

ICD-10 Classifications

Crohn disease, unspecified
Other Crohn disease
Crohn disease of large intestine
Crohn disease [regional enteritis]
Crohn disease of small intestine

Data Source

ClinicalTrials.gov

NCT06299631

Non-Device Trial