Comparison of the Occurrence of Postoperative Complications Between Robotic and Laparoscopic Surgery in Revision Bariatric Surgery
Recruiting · NCT07180316 · Observational (researchers observe without assigning treatment)
View the official record on ClinicalTrials.gov →What this trial is about
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
Who can take part
Age range
18 Years to 70 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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
Where it is running
2 locations listed.
- Hôpital Privé Jean Mermoz - Lyon, France
- Hôpital privé de la Loire - Ramsay Santé - Saint-Etienne, France