Evaluating outcomes of bariatric surgery for obesity

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study involves a prospective database established at the University Hospital of Strasbourg, focusing on candidates for obesity surgery. It aims to assess the quality of life of patients who underwent Roux en Y gastric bypass, comparing those with internal hernias to those with uncomplicated recovery. Patients are evaluated by a multidisciplinary team and undergo various preoperative assessments, with data collected on surgical outcomes and follow-up. The study utilizes anonymized personal data for research purposes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* patient \>18 years old
* BMI \> 35 kg/m²

Exclusion Criteria:

* Incapacity of giving an informed consent

Where it's running

• Service de Chirurgie Digestive et Endocrinienne
  Strasbourg, France Recruiting

Study contacts

• Study coordinator: Didier Mutter, MD, PhD
• Email: didier.mutter@chru-strasbourg.fr
• Phone: +33 (0)3 90 11 90 41

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.