Obesity Clinical Trial
— microbariaOfficial title:
Modification of Human Gut Microbiota in Massive Obesity After Bariatric Surgery: the Role of Energetic Restriction
NCT number | NCT01454232 |
Other study ID # | P100111 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 7, 2011 |
Est. completion date | September 14, 2018 |
Verified date | March 2019 |
Source | Assistance Publique - Hôpitaux de Paris |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Gut microbiota ecology is altered in obesity and could link obesity and its complications.
Bariatric surgery enables a major and sustained weight loss therefore improving obesity
related disease.
the investigators primary aim is to evaluate gut microbiota adaptation to weight loss and the
specific role of energetic restriction. Furthermore we aim to compare gut flora of obese
patients post bariatric surgery to that of lean healthy volunteers.
Thus, the investigators plan to compare gut microbiota from 140 obese individuals before and
after either restrictive (gastric banding) procedures or gastric bypass procedures to that of
40 lean healthy volunteers at baseline.
Status | Completed |
Enrollment | 140 |
Est. completion date | September 14, 2018 |
Est. primary completion date | September 14, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Obese group Inclusion criteria : - Obesity with BMI> 40 kg/m² or obesity with BMI between 35 and 40 kg/M² with comorbidities (OSA, type 2 diabetes, hypertension etc…) - Age: 18-65 - women - weight stable for three months preceding surgery Exclusion criteria : - Inflammatory disease - Pregnancy - Lactose intolerance - Antibiotherapy in the three months preceding surgery - cancer - Drugs (AINS) Healthy group Inclusion criteria : - 19<BMI<25kg/m² - Age: 18-65 - women - non diabetic Exclusion criteria : - Inflammatory disease - Pregnancy - Antibiotherapy in the two months preceding the visit - pregnancy - Drugs (AINS) in the 48h preceding the visit |
Country | Name | City | State |
---|---|---|---|
France | Pitié Salpêtrière Hospital | Paris |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique - Hôpitaux de Paris |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Analyse changes early, medium and long term changes in gut microbiota composition in a kinetic manner | at 1, 3 and 12 months after surgery | ||
Primary | Compare gut microbiota kinetic changes in obese to gut microbiota healthy volunteers | at 1, 3 and 12 months after surgery in the obese group and compare it to baseline in lean subjects | ||
Secondary | Establish early, medium and long term changes in insulin sensitivity and GLP1 secretion profile after oral glucose load and look for potential associations between these changes and gut microbiota composition | 1, 3 and 12 months after surgery | ||
Secondary | Establish early, medium and long term changes in systemic and adipose tissue inflammation and look for potential associations between gut microbiota composition and inflammation modification | 1, 3 and 12 months after surgery | ||
Secondary | Establish early, medium and long term changes in body composition and look for potential associations between these changes and gut microbiota modifications | 1, 3 and 12 months after surgery | ||
Secondary | Establish early, medium and long term changes in nutritional blood sample concentrations and look for a potential association between gut microbiota modifications. | 1, 3, 12 months after surgery | ||
Secondary | Establish early, medium and long term improvement in obesity related disease (reducing the number of treatments and the need for PPC use) and look for potential association with gut microbiota modification | 1, 3 and 12 months after surgery |
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