Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
161 participants
OBSERVATIONAL
2024-04-24
2026-06-15
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Adult patients with digestive surgery
Patients who have planned abdominal surgery
Post-operative ileus surgery
Collection of ileus events, items of IFEED score and surgical complications
Interventions
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Post-operative ileus surgery
Collection of ileus events, items of IFEED score and surgical complications
Eligibility Criteria
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Inclusion Criteria
* Colorectal cancer
* Chronic inflammatory bowel disease
* Colonic diverticulosis.
Exclusion Criteria
* Patient presenting during hospitalization with an ileus secondary to another intra-abdominal complication.
* Patient cared for in an emergency
* Hepatic resection or other associated metastatic site
* Multiple digestive resection
* Colorectal anastomosis less than 7 cm from the anal margin (below the Pouch of Douglas)
* Patient with American Society of Anesthesiologists physical status (ASA) score \> 2
* Patient with an Eastern Cooperative Oncology Group (ECOG) Performance Status Scale \>2
* Pregnant or breastfeeding women
* Patient under a protection regime for adults (guardianship, curators, safeguard of justice)
18 Years
ALL
No
Sponsors
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Institut National de la Santé Et de la Recherche Médicale, France
OTHER_GOV
University Hospital, Toulouse
OTHER
Responsible Party
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Principal Investigators
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Guillaume LE COSQUER, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Toulouse
Locations
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CHU de Toulouse
Toulouse, , France
INSERM
Toulouse, , France
Countries
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Central Contacts
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Facility Contacts
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Guillaume LE COSQUER, MD
Role: primary
Etienne BUSCAIL, MD-PhD
Role: primary
Other Identifiers
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2022-A02834-39
Identifier Type: OTHER
Identifier Source: secondary_id
RC31/22/0491
Identifier Type: -
Identifier Source: org_study_id