Obesity Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 or older
- People who are able to read and understand the study information and consent form
- People with a BMI over 35 who also have at least one other related health condition, or people with a BMI over 40
- People whose case for weight-loss digestive surgery has been approved through a specialist multidisciplinary team meeting and by the relevant health insurance authority (CPAM)
- People who are members of a social security scheme in France
- People who have given their signed agreement to participate in the study
- For the GLP-1 medication group: people who have been taking a GLP-1 analogue medication for at least 3 months
- For the comparison group: people who have never taken a GLP-1 analogue medication
Who may not be able to join:
- Women who are pregnant or currently breastfeeding
- People who are under legal guardianship or considered legally vulnerable
- People who are currently deprived of their liberty (for example, those who are incarcerated)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Iannelli Antonio, PhD, Clinique Parc Impérial, Service de Chirurgie Digestive
Phone: +3349209220
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Rate of oxytocin
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.