Comparison of Gastric By-Pass and Optimized Medical Treatment in Obese Diabetic Patients (DIABSURG)
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Purpose
The objectives are to compare the results of the Gastric By-Pass (GBP) to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of mortality, weight loss, glycemic control, quality of life, cost, cost-effectiveness and cost utility of these two strategies.
| Condition | Intervention | Phase |
|---|---|---|
|
Obesity Diabetes |
Procedure: Gastric By-Pass Drug: optimized medical management |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Comparison of Gastric By-Pass and Optimized Medical Treatment in Obese Diabetic Patients in Terms of Mortality, Glycemic Control, and Cost Effectiveness - Prospective, Multicenter, Randomized Study |
- overall mortality [ Time Frame: 5 years ] [ Designated as safety issue: No ]to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of mortality
- overall mortality [ Time Frame: 7 years ] [ Designated as safety issue: No ]The objectives are to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of mortality
- overall mortality [ Time Frame: 10 years ] [ Designated as safety issue: No ]The objectives are to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of mortality
- weight loss [ Time Frame: 2 years ] [ Designated as safety issue: No ]The objectives are to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of weight loss
- glycemic control [ Time Frame: 2 years ] [ Designated as safety issue: No ]The objectives are to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of glycemic control
- quality of life [ Time Frame: 2 years ] [ Designated as safety issue: No ]The objectives are to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of quality of life
- cost, cost-effectiveness and cost utility [ Time Frame: 2 years ] [ Designated as safety issue: No ]The objectives are to compare the results of the GBP to that of optimized medical therapy in patients with obesity and poorly controlled type 2 diabetes in terms of cost, cost-effectiveness and cost utility of these two strategies.
| Estimated Enrollment: | 490 |
| Study Start Date: | February 2011 |
| Estimated Study Completion Date: | September 2021 |
| Estimated Primary Completion Date: | September 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Gastric By-Pass
group treated with Gastric By-Pass
|
Procedure: Gastric By-Pass
Bariatric surgery laparoscopic Roux-en-Y Gastric Bypass (RYGBP)
Other Name: RYGBP
|
|
Active Comparator: optimized medical management
group receiving an optimized medical management
|
Drug: optimized medical management
group receiving an optimized medical management, among patients with obesity and poorly controlled type 2 diabetes
Other Name: optimized medical management
|
Detailed Description:
Optimizing the management of type 2 diabetes (T2D) will remain a major public health concern for decades to come. T2DM has already affected 4% of the French population and generates each year over 12 billion euros of expenditure. By combining therapies, oral and/or injectable (insulin or analogues of GLP-1), the current management of T2DM provides two thirds of patients with a satisfactory metabolic control (HbA1c < 7%) and reduced incidence of cardiovascular complications. Its effect on mortality, however, remains more limited, presumably because of the persistence of other cardiovascular risk factors. A recent study has confirmed that French patients with T2DM present an overall mortality risk significantly higher than the general population. In France, this group registered a mortality of 32 deaths per 1000 persons.
Bariatric surgery is now a recognized method for the treatment of severe obesity. It allows for the permanent loss of at least 50% of initial excess weight. In obese patients, this surgery is also associated with a significant reduction in cardiovascular risk factors and particularly T2D. A recent meta-analysis of retrospective studies available suggests that surgery results in remission of T2DM in over 75% of cases. The only prospective randomized study showed that gastric restriction by placing a gastric band, provides better glycemic control than just medical treatment in obese patients with recently discovered T2DM. The gastric by-pass (GBP) which also includes an intestinal by-pass, seems to have an even higher metabolic efficiency than gastric bypass alone. In patients with T2DM, the GBP restores postprandial insulin secretion independently of weight loss. Despite the significant morbidity of the intervention, long-term results seem broadly supportive of the GBP. In a large case-control study, GBP was associated with a decrease of 90% of deaths related to diabetes. In a controlled study conducted in surgical candidates obese diabetics, the GBP decreased the overall world mortality by 75% after 6 years. Despite these very encouraging data, the GBP is now proposed to only a small proportion (< 1%) of patients likely to benefit from the procedure.
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Type 2 diabetes mellitus with HbA1c > 7.5 %
- Body mass index > 35 and < 50 kg/m2
- Candidate for Gastric By-Pass
- Treatment with GLP1 (glucagon-like peptide) analogue or insulin
Exclusion Criteria:
- Contraindication to bariatric surgery
- Pregnancy
- Affiliation of health care assurance
- Psychiatric disorders
Contacts and Locations| Contact: Francois Pattou, Professor | 00 33 3 20 44 42 73 | fpattou@iv-lille2.fr |
| France | |
| University Hospital of Lille | Recruiting |
| Lille, Nord, France, 59000 | |
| Contact: Violeta Raverdy, MD 00 33 3 20 44 59 62 vraverdi@univ-lille2.fr | |
| Sub-Investigator: Pierre Fontaine, Professor | |
| Study Director: | Francois Pattou, Professor | University Hospital of Lille |
More Information
No publications provided
| Responsible Party: | Francois Pattou, Professor of Medecine, University Hospital, Lille |
| ClinicalTrials.gov Identifier: | NCT01501201 History of Changes |
| Other Study ID Numbers: | 2010_07/1019 |
| Study First Received: | December 20, 2011 |
| Last Updated: | September 20, 2012 |
| Health Authority: | France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) |
Keywords provided by University Hospital, Lille:
|
Obesity Diabetes Bariatric Surgery |
Additional relevant MeSH terms:
|
Diabetes Mellitus Obesity Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases |
Overnutrition Nutrition Disorders Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 19, 2013