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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15+
SponsorUniversity Hospital, Montpellier

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Unable to follow the patient in the long term (foreign patients, surgical use ...)

Inability to follow in the long run

Trial design

Design model

Single group

Treatments tested in this trial

  • Bariatric surgery

    Procedure/Surgery

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

Treatment groups

750 Participants
are divided into 1 treatment group
Group A: Group/CohortOther 1 intervention

Trial outcomes

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

Other outcomes

Sponsors and contacts

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