Low Stable Pressure Pneumoperitoneum in Colorectal Surgery (CROSS STUDY)
NCT ID: NCT06154785
Last Updated: 2025-08-01
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
300 participants
OBSERVATIONAL
2023-12-15
2025-09-30
Brief Summary
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Detailed Description
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However, other factors may influence the outcomes of the low-pressure pneumoperitoneum such as the use of humidification and warming gaz, robotic or microsurgical instrumentation, neuromuscular blockade, patient positioning, pre-stretching of the abdominal wall, ventilation-induced changes, and probably individual patient factors like obesity. These parameters could not be separately tested in randomized trial. We should consider all these parameters in a prospective international registry in order to optimize the benefit of low-pressure pneumoperitoneum in post-operative recovery.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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International cohort
This is an international cohort (France and other international centers) which consists of including patients undergoing colorectal surgery performed at low pressure for benign or malignant pathology.This stage 2b cohort study is a pilot study assessing the best operative association with stable low-pressure pneumoperitoneum in order to optimize postoperative outcomes after mini invasive colorectal surgery.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Colonic resection (right or left, subtotal or total) performed for benign or malignant pathology
* Rectal resection with or without stoma for benign or malignant pathology
* Laparoscopic or robotic procedure
* Surgery under low stable pressure pneumoperitoneum with AirSeal
* Patient who benefits by medicare system
* Oral agreement after reading information letter
Exclusion Criteria
* Associated resection (except appendectomy or liver biopsy)
* Transverse colectomy
* Emergency procedure
* Pelvic sepsis
* Pregnancy or breast feeding period
* Legal incapacity or physical, psychological social or geographical status interfering with the patient's ability to agree to participate in the study
* Persons deprived of liberty or under guardianship
18 Years
ALL
No
Sponsors
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Bordeaux Colorectal Institute Academy
OTHER
Responsible Party
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Locations
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Universitair Ziekenhuis
Jette, Brussels Capital, Belgium
Hôpital Jean Minoz
Besançon, , France
Clinique Tivoli-Ducos - Bordeaux Colorectal Institute
Bordeaux, , France
Hôpital Albert Michallon
La Tronche, , France
Hôpital Bicêtre
Le Kremlin-Bicêtre, , France
Hôpital Nord-Marseille
Marseille, , France
Clinique Hartmann
Neuilly-sur-Seine, , France
Hopital Saint-Louis
Paris, , France
Hôpital Saint-Antoine
Paris, , France
Hôpital Européen Georges Pompidou
Paris, , France
Hôpital Lyon Sud
Pierre-Bénite, , France
Hopital Charles Nicolle
Rouen, , France
St. Georg Klinikum Eisenach
Eisenach, , Germany
Division of Colon and Rectal Surgery
Milan, , Italy
Academic Medical Center
Amsterdam, , Netherlands
Hospital General Universitario Gregorio
Madrid, , Spain
Hôpitaux Universitaires de Genève
Geneva, , Switzerland
Nhs Fundation Trust
Manchester, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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B.C.I.A 2023/01
Identifier Type: -
Identifier Source: org_study_id
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