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RecruitingNCT02310178BAREVALUpdated Jun 22, 2026

Obesity Cohort : Medical Follow-up of Severe or Morbid Obese Patients Undergoing Bariatric Surgery

An interventional study of Bariatric surgery in Obesity, Morbid and Bariatric Surgery Candidate, sponsored by University Hospital, Montpellier. Recruiting at 1 site in France. Open to participants aged 15 Years and older. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by University Hospital, Montpellier · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 2 years 5 months after the study started (first participant enrolled May 2012, registered Oct 2014).
  • Started May 2012; still recruiting 14 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
750
Allocation
Not applicable
Ages
15 Years and older
Sex
All
01

Study summary

The aim of this cohort is to evaluate the follow-up of morbidly obese patients treated by several types of bariatric procedures. In addition, this study could lead to the development of clinical trials on assessment of the bariatric surgery impact.

Read the detailed description

The main objective is to prospectively evaluate long-term efficiency of bariatric surgery in terms of weight loss. Moreover, this cohort wants to assess the long-term effectiveness of bariatric surgery on comorbidities and quality of life, the medical and economic impact of bariatric surgery (before-after comparison using data from health insurance), estimates the incidence of mortality and morbidity of bariatric surgery and to finish describe the evolution of patients in case of new-surgery. From a methodological point of view, the Obesity cohort is a prospective cohort study, single-center, open, with aftercare performed during life of patients. The number of inclusions is to 1500 patients. After surgery , patients will be followed at least 4 visits the first year and at least 2 visits a year then. The recommendations of the french health ministry (HAS), the frequency of visits may be increased according to the patient's progress. Follow-up visits of patients after bariatric surgery will be performed by physicians or surgeons of the multidisciplinary team responsible for the care of the patient (digestive and reconstructive surgery, anesthesiology, endocrinology, medical imaging, gastroenterology, immunology and physiology) . It will be insured for life, obesity is a chronic disease and because of the risk of late complications.

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Conditions studied

  • Obesity, Morbid
  • Bariatric Surgery Candidate

Keywords

  • weight loss
  • sleeve gastrectomy
  • gastric bypass
  • gastric banding
  • bariatric procedures
  • cohort
  • morbid obesity
  • medical and economical impact
  • severe obesity
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In context

Obesity, Morbid

922 studies on the registry are indexed under Obesity, Morbid; 172 are open to participants now.

This study's planned enrollment of 750 is above the median of 60 across 590 interventional studies indexed under Obesity, Morbid.

Browse Obesity, Morbid studies →

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
15 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

Exclusion Criteria:

  • Unable to follow the patient in the long term (foreign patients, surgical use ...)
  • Inability to follow in the long run
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
750 participants (estimated)

Study arms

  • Other
    Group/Cohort

    all of the current bariatric surgeries are allowed in this prospective cohort study

    Procedure: Bariatric surgery

Interventions

  • ProcedureBariatric surgery

    all of the current bariatric surgeries are allowed in this prospective cohort study

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What researchers measure

Primary outcomes

  1. Assessment of the long-term efficiency of bariatric surgery on weight loss

    Assessment of weight loss

    Time frame: Change from intervention to 5 years

Secondary outcomes

  1. Assessment of the long-term efficiency of bariatric surgery on diabetes

    Assessment of blood glucose, HbA1c and diabetes medications

    Time frame: Change from intervention to 5 years

  2. Assessment of the long-term efficiency of bariatric surgery on High Blood Pressure

    Assessment of Systolic Blood Pressure and blood pressure medications

    Time frame: Change from intervention to 5 years

  3. Assessment of the long-term efficiency of bariatric surgery on dyslipidemia

    Assessment of cholesterolemia and triglyceridemia and dyslipidemia medications

    Time frame: Change from intervention to 5 years

  4. Assessment of the long-term efficiency of bariatric surgery on rheumatism

    Assessment of rheumatism medications

    Time frame: Change from intervention to 5 years

  5. Assessment of the long-term efficiency of bariatric surgery on respiratory pathologies

    Assessment of respiratory pathologies medications

    Time frame: Change from intervention to 5 years

  6. Assessment of the long-term efficiency of bariatric surgery on sleep apnea syndrome

    polysomnography tests

    Time frame: Change from intervention to 3 months

  7. Assessment of the long-term efficiency of bariatric surgery on quality of life

    Assessment of quality of life questionnaires (SF36 and BAROS)

    Time frame: Change from intervention to 5 years

  8. Assessment of medico-economic impact of bariatric surgery

    Comparison of health insurance data

    Time frame: Change from intervention to 5 years

  9. Assessment of mortality of bariatric surgery

    Assessment of the date of death

    Time frame: Change from intervention to 5 years

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Study locations

1 of 1 sites recruiting
  • CHRU - Hôpital Saint Eloi
    Montpellier, 34295, France
    Recruiting
08

References and documents

Publications

  • Saux P, Bauvin P, Raverdy V, Teigny J, Verkindt H, Soumphonphakdy T, Debert M, Jacobs A, Jacobs D, Monpellier V, Lee PC, Lim CH, Andersson-Assarsson JC, Carlsson L, Svensson PA, Galtier F, Dezfoulian G, Moldovanu M, Andrieux S, Couster J, Lepage M, Lembo E, Verrastro O, Robert M, Salminen P, Mingrone G, Peterli R, Cohen RV, Zerrweck C, Nocca D, Le Roux CW, Caiazzo R, Preux P, Pattou F. Development and validation of an interpretable machine learning-based calculator for predicting 5-year weight trajectories after bariatric surgery: a multinational retrospective cohort SOPHIA study. Lancet Digit Health. 2023 Oct;5(10):e692-e702. doi: 10.1016/S2589-7500(23)00135-8. Epub 2023 Aug 29. PubMed 37652841 ↗
  • Nocca D, Galtier F, Taleb S, Picot MC, Jaussent A, Silvestri M, Lefebvre P, de Jong A, Gautier T, Loureiro M, Nedelcu M. Peri-operative Morbidity of Nissen Sleeve Gastrectomy: Prospective Evaluation of a Cohort of 365 Patients, Beyond the Learning Curve. Obes Surg. 2022 Jul;32(7):1-7. doi: 10.1007/s11695-022-06066-0. Epub 2022 May 7. PubMed 35524904 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02310178
Lead sponsor
University Hospital, Montpellier
Responsible party
Sponsor
First posted
Dec 8, 2014
Start date
May 21, 2012
Primary completion
Dec 2026 (estimated)
Completion
Dec 2028 (estimated)
Last update
Jun 22, 2026

Study contacts

David NOCCA, PUPH
Contact
d-nocca@chu-montpellier.fr
0467337731 ext. +33

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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