Observing outcomes of bariatric surgery patients

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 cohort study aims to collect clinical data from patients who have undergone bariatric surgery or experienced complications related to such procedures. The focus is on improving follow-up care and assessing outcomes related to weight loss and complication rates. By gathering and analyzing this data, the study seeks to enhance understanding of the long-term effects of bariatric surgery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* History of bariatric surgery procedure

Exclusion Criteria:

* Patients \< 16 years
* Patients \> 80 years

Where it's running

• Department of Digestive Surgery, University Hospital of Edouard Herriot, Hospices Civils de Lyon
  Lyon, France Recruiting

Study contacts

• Principal investigator: Maud ROBERT, Pr — Department of Digestive Surgery, University Hospital of Edouard Herriot, Hospices Civils de Lyon
• Study coordinator: Maud ROBERT, Pr
• Email: maud.robert@chu-lyon.fr
• Phone: (0)4 72 11 62 63

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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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.