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Study of Bariatric Surgery

NCT02857179 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2016-08-05

No results posted yet for this study

Summary

The aim of this cohort study is to collect prospectively clinical data on all the patients admitted in the investigators department for bariatric surgery or for any complication of a bariatric procedure. The investigators goal is not only to improve the follow-up but also to assess and publish the investigators results regarding weight loss and the complication rate.

Conditions

  • Bariatric Surgery

Interventions

PROCEDURE

bariatric surgery

gastric bypass Or gastric banding Or Biliopancreatic diversion with duodenal switch Or sleeve gastrectomy Or endoscopic procedure (Endobarrier,…)

Sponsors & Collaborators

  • Hospices Civils de Lyon

    lead OTHER

Principal Investigators

  • Maud ROBERT, Pr · Department of Digestive Surgery, University Hospital of Edouard Herriot, Hospices Civils de Lyon

Eligibility

Min Age
16 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2032-11-30
Completion
2032-11-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02857179 on ClinicalTrials.gov