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Clinical Trial Summary

In this research, we hypothesize that post-operative monitoring implemented with a connected scale after the 1st year (weight nadir period) post obesity surgery (i.e. sleeve and RYGB) would reduce the percentage of patients with excessive weight regain (>10% regain of lost weight) by improving the quality of follow-up and long-term results. To do this, we are carrying out a comparative study on 182 patients, controlled, randomized per patient, ratio 1/1, open, in two parallel arms. Patients will be followed for 12 months and divided into one of the following two groups: - Control group: Standard follow-up - Interventional group: Standard follow-up + weekly weighing with the "Body Comp Pro" connected scale During their follow-up period, patients in the intervention group will have to weigh themselves at least once a week using the "Body Comp Pro" connected scale. The information will be transmitted to the investigation team via a secure platform available 24 hours a day. Alerts will be generated from a weight regain > 5% of the baseline weight, allowing early management of weight regain.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06133413
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact Laurent GENSER, Dr
Phone 01.42.17.56.14
Email laurent.genser@aphp.fr
Status Not yet recruiting
Phase N/A
Start date May 2024
Completion date September 2025

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