Evaluating outcomes of bariatric surgery for obesity
An Evaluation of the Outcomes of Bariatric Surgery - a Cohort Study Internal Hernia After Laparoscopic Roux-en-Y Gastric Bypass: an Evaluation of the Impact on the Postoperative Course and a Quality of Life Case-control Study
This study looks at how bariatric surgery affects the quality of life for people with obesity, comparing those who have complications like internal hernias to those who recover without issues.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | IHU Strasbourg Academic / other |
| Locations | 1 site (Strasbourg) |
| Trial ID | NCT02811900 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old with a BMI greater than 35 kg/m² seeking bariatric surgery.
Not a fit: Patients unable to provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of the quality of life outcomes following different bariatric surgical procedures.
How similar studies have performed: Other studies have shown success in evaluating quality of life outcomes post-bariatric surgery, indicating this approach is supported by existing research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patient \>18 years old * BMI \> 35 kg/m² Exclusion Criteria: * Incapacity of giving an informed consent
Where this trial is running
Strasbourg
- 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
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.