NCT07180316 Comparison of the Occurrence of Postoperative Complications Between Robotic and Laparoscopic Surgery in Revision Bariatric Surgery
| NCT ID | NCT07180316 |
| Status | Recruiting |
| Phase | — |
| Sponsor | GCS Ramsay Santé pour l'Enseignement et la Recherche |
| Condition | Obesity and Overweight |
| Study Type | OBSERVATIONAL |
| Enrollment | 200 participants |
| Start Date | 2025-06-17 |
| Primary Completion | 2029-06-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 200 participants in total. It began in 2025-06-17 with a primary completion date of 2029-06-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
In a population of patients undergoing bariatric revision surgery with conversion to RYGB and divided into two groups according to the surgical protocol: Group 1: robotic surgery Group 2: laparoscopy The primary objective of the study is to compare the rates of postoperative complications between the two groups, classified according to the Clavien Dindo classification. The secondary objectives are to compare between the groups: * Total duration of the surgical procedure, stay in the emergency room, and hospitalization * Postoperative pain * Adverse events * Weight loss * Improvement in comorbidities
Eligibility Criteria
Inclusion Criteria: * Patients aged 18 to 70 years, * Patients who have been informed of the objectives and conditions of the study and who have not objected to the collection of their data * Patients who are candidates for or have undergone revision bariatric surgery with conversion to RYGB (post-ring, post-sleeve, post-OAGB) Exclusion Criteria: * Pregnant patient * Patient unable to understand information: dementia, psychosis, impaired consciousness, language difficulties
Frequently Asked Questions
Who can join the NCT07180316 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Obesity and Overweight. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07180316 currently recruiting?
Yes, NCT07180316 is actively recruiting participants. Visit ClinicalTrials.gov or contact GCS Ramsay Santé pour l'Enseignement et la Recherche to inquire about joining.
Where is the NCT07180316 trial being conducted?
This trial is being conducted at Lyon, France, Saint-Etienne, France.
Who is sponsoring the NCT07180316 clinical trial?
NCT07180316 is sponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche. The trial plans to enroll 200 participants.
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