Observing outcomes of bariatric surgery patients
Prospective Cohort Study Monitoring Patients Undergoing Bariatric Surgery
This study looks at the experiences of people who have had bariatric surgery to see how well they are doing with weight loss and any complications they might face.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 16 Years to 80 Years |
| Sex | All |
| Sponsor | Hospices Civils de Lyon Academic / other |
| Locations | 1 site (Lyon) |
| Trial ID | NCT02857179 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are individuals who have a history of undergoing bariatric surgery.
Not a fit: Patients under 16 years or over 80 years old may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved follow-up care and better management of complications for bariatric surgery patients.
How similar studies have performed: Other studies have shown success in observing outcomes of bariatric surgery, indicating that this approach is supported by prior research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * History of bariatric surgery procedure Exclusion Criteria: * Patients \< 16 years * Patients \> 80 years
Where this trial is running
Lyon
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.