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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04002921
Other study ID # CHD 086-19
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 24, 2019
Est. completion date November 10, 2025

Study information

Verified date July 2023
Source Centre Hospitalier Departemental Vendee
Contact Agnes DORION
Phone 0251446380
Email agnes.dorion@ght85.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anastomotic leakage is the major postoperative complication in right colectomy. Evaluation of calcification on coeliac trunk and mesenteric arteries on the preoperative CT scan could allow the identification of patient at-risk of postoperative complications. A monocentric retrospective study performed at CHD Vendée concluded than a calcification score over or equal to 3 was associated with a higher risk of developping an anastomotic leakage. The aim of this prospective multicentric study is to validate a calcification score based on preoperative CT scan analysis and focussing at coeliac trunk and mesenteric arteries.This study will involve patients operated on with a scheduled right colectomy.


Recruitment information / eligibility

Status Recruiting
Enrollment 1100
Est. completion date November 10, 2025
Est. primary completion date November 10, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years old - Scheduled right colectomy with restoration of digestive continuity - Patient who has had or will have a preoperative abdominal-pelvic CT scan with or without contrast injection - Patient with the ability to understand the protocol and agree to participate in the study. - Affiliated with a social security system Exclusion Criteria: - Patient requiring a right colectomy or ileocaecal resection for chronic inflammatory bowel disease or on long-term corticosteroid therapy - Patient with a history of colic resection - Patient under guardianship, curatorship, or deprived of liberty - Pregnant, postpartum or breastfeeding women - Minor patients

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU Angers Angers
France Hopital privé de Sévigné Cesson-Sévigné
France CH de Challans Challans
France CH de Cholet 1 rue Marengo Cholet
France Centre Hospitalier de Fougères Fougères
France CHD Vendée La Roche sur Yon
France Centre Hospitalier de la Rochelle La Rochelle
France Centre Hospitalier du Mans Le Mans
France Clinique Mutualiste de la Porte de l'Orient Lorient
France CHU de Nantes Nantes
France Hopital privé des Cotes d'Armor Plérin
France Clinique La Sagesse Rennes
France Centre Hospitalier de Saint Brieuc Saint-Brieuc
France Clinique Mutualiste de l'Estuaire Saint-Nazaire
France Centre Hospitalier Bretagne Atlantique Vannes
France Hôpital privé Océane Vannes

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Departemental Vendee

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total calcification score associated with the occurrence of anastomotic leakage Sum of the calcification scores of the following 4 segments (=3) associated with the occurrence of anastomotic leakage within 6 weeks postoperatively.
4 segments:
Ostium of celiac artery
Ostium of superior mesenteric artery
first segment of superior mesenteric artery
distal segment of superior mesenteric artery Each segment will be assigned a score between 0 and 2. Total score range : 0-8
6 weeks after surgery
Secondary Calcification score of each segment associated with the occurrence of anastomotic leakage 4 segments:
Ostium of celiac artery
Ostium of superior mesenteric artery
first segment of superior mesenteric artery
distal segment of superior mesenteric artery Each segment will be assigned a score between 0 and 2.
6 weeks after surgery
Secondary Morbidities defined according to Clavien-Dindo classification Morbidities defined according to Clavien-Dindo classification occurring at 6 weeks postoperatively 6 weeks after surgery
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