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Taking people in FranceNo phase

Comparing Robotic and Laparoscopic Surgery for Revision Weight-Loss Surgery Complications

Compares robotic and keyhole surgery for revising earlier weight-loss surgery in adults.

Plain-language title generated from the registry record
Registry title: Comparison of the Occurrence of Postoperative Complications Between Robotic and Laparoscopic Surgery in Revision Bariatric Surgery

Key facts

Where
Lyon and Saint-Etienne, FranceSee the 2 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 70 years old?

Source: NCT07180316, who can take part

Where in France

  • Hôpital Privé Jean MermozLyon, FranceTaking people
  • Hôpital privé de la Loire - Ramsay SantéSaint-Etienne, FranceNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
GCS Ramsay Santé pour l'Enseignement et la Recherche
Trial code
NCT07180316
Record updated
18 September 2025
Original description
In a population of patients undergoing bariatric revision surgery with conversion to RYGB and divided into two groups according to the surgical protocol:Read full original descriptionShow less

Comparison of the Occurrence of Postoperative Complications Between Robotic and Laparoscopic Surgery in Revision Bariatric Surgery

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

Inclusion: 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: Patient unable to understand information: dementia, psychosis, impaired consciousness, language difficulties; Pregnant patient.

ClinicalTrials.gov NCT07180316