Long-term follow-up of severely obese patients after bariatric surgery
Official title: Obesity Cohort : Medical Follow-up of Severe or Morbid Obese Patients Undergoing Bariatric Surgery
Run by University Hospital, Montpellier · NCT02310178 · Data updated 2026-11-12
This study is trying to see how well different types of weight loss surgery work for severely obese patients over the long term and how it affects their health and quality of life.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 15 Years and up |
| Sex | All |
| Enrollment | 750 (estimated) |
| Sponsor | University Hospital, Montpellier Academic / other |
| Locations | 1 site (Montpellier) |
| Status | Recruiting |
| Started | May 21, 2012 |
| Main results expected | December 2026 |
| Study ends | December 2028 |
| Registry record updated | June 22, 2026 |
| Trial ID | NCT02310178 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are morbidly obese patients who are undergoing bariatric surgery at CHU Montpellier and can commit to long-term follow-up.
✕Probably not a fit
Patients who are unable to participate in long-term follow-up or are not treated at CHU Montpellier may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This cohort aims to evaluate the long-term effectiveness of various bariatric surgery procedures on morbidly obese patients. It will assess weight loss outcomes, improvements in comorbidities, quality of life, and the medical and economic impacts of surgery. Patients will be followed for life with regular visits to a multidisciplinary team, ensuring comprehensive care and monitoring of potential complications. The study will include 1500 patients treated at CHU Montpellier, with a structured follow-up schedule to gather extensive data on their progress.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the long-term benefits of bariatric surgery for morbidly obese patients.
How similar studies have gone: Other studies have shown positive outcomes with similar approaches in evaluating bariatric surgery, indicating a potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Only be considered in patients operated and followed at CHU Montpellier with bariatric surgery * Patients treated by bariatric surgery on CHU Montpellier * Agreed to participate to the study by signing an informed consent * Eligible to health insurance Exclusion Criteria: * Unable to follow the patient in the long term (foreign patients, surgical use ...) * Inability to follow in the long run
Where it's running
-
CHRU - Hôpital Saint Eloi
Montpellier, France Recruiting
Study contacts
- Study coordinator: David NOCCA, PUPH
- Email: d-nocca@chu-montpellier.fr
- Phone: 0467337731
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Understanding genetic factors that affect weight loss after bariatric surgery
This study is trying to find out if certain genes can help predict how well people with severe obesity will lose weight after having bariatric surgery.
-
Identifying predictors of weight loss and metabolic health after bariatric surgery
This study is trying to find out what factors can help predict how well people with insulin resistance will lose weight and improve their health after having bariatric surgery.
-
Understanding why some patients don't lose weight after bariatric surgery
This study is trying to find out why some people don’t lose as much weight as expected after bariatric surgery, focusing on the role of gut hormones to help improve their results.
-
Survey on bariatric surgery for adolescents
This study is trying to see how well laparoscopic adjustable gastric banding works for teenagers aged 14-20 who are having bariatric surgery, focusing on weight loss and any health issues that might come up.
-
Registry for bariatric surgery quality control
This study is setting up a registry to track the results and safety of bariatric surgery for people who are severely obese to help improve surgical practices.
-
Glycemic variability after SASI versus Roux-en-Y gastric bypass
This trial tests whether SASI or Roux-en-Y gastric bypass leads to different glucose fluctuations in adults with severe obesity using continuous glucose monitoring.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.