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Comparison of Gastric By-Pass and Optimized Medical Treatment in Obese Diabetic Patients (DIABSURG)

Primary Purpose

Obesity, Diabetes

Status
Recruiting
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Gastric By-Pass
optimized medical management
Sponsored by
University Hospital, Lille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Obesity, Diabetes, Bariatric Surgery

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University Hospital of LilleRecruiting
  • Centre Hospitalier Regional D' AngersRecruiting
  • Hopital de Bois-Guillaume Chu RouenRecruiting
  • Hu Ouest Site Ambroise Pare Aphp -Recruiting
  • Hopital Jeanne D'Arc Chu NancyRecruiting
  • Hopital Lyon Sud - Hcl - Pierre BeniteRecruiting
  • Hopital Lapeyronie Chu MontpellierRecruiting
  • Hu Pitie Salpetriere AphpRecruiting
  • Hopital Larrey Chu ToulouseRecruiting
  • Ch ValenciennesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Gastric By-Pass

optimized medical management

Arm Description

group treated with Gastric By-Pass

group receiving an optimized medical management

Outcomes

Primary Outcome Measures

overall mortality
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

Secondary Outcome Measures

overall mortality
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
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
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
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
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
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.

Full Information

First Posted
December 20, 2011
Last Updated
February 6, 2023
Sponsor
University Hospital, Lille
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1. Study Identification

Unique Protocol Identification Number
NCT01501201
Brief Title
Comparison of Gastric By-Pass and Optimized Medical Treatment in Obese Diabetic Patients
Acronym
DIABSURG
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
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 8, 2011 (Actual)
Primary Completion Date
September 2029 (Anticipated)
Study Completion Date
September 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Diabetes
Keywords
Obesity, Diabetes, Bariatric Surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
490 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gastric By-Pass
Arm Type
Experimental
Arm Description
group treated with Gastric By-Pass
Arm Title
optimized medical management
Arm Type
Active Comparator
Arm Description
group receiving an optimized medical management
Intervention Type
Procedure
Intervention Name(s)
Gastric By-Pass
Other Intervention Name(s)
RYGBP
Intervention Description
Bariatric surgery laparoscopic Roux-en-Y Gastric Bypass (RYGBP)
Intervention Type
Drug
Intervention Name(s)
optimized medical management
Intervention Description
group receiving an optimized medical management, among patients with obesity and poorly controlled type 2 diabetes
Primary Outcome Measure Information:
Title
overall mortality
Description
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
Time Frame
5 years
Secondary Outcome Measure Information:
Title
overall mortality
Description
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
Time Frame
7 years
Title
overall mortality
Description
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
Time Frame
10 years
Title
weight loss
Description
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
Time Frame
2 years
Title
glycemic control
Description
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
Time Frame
2 years
Title
quality of life
Description
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
Time Frame
2 years
Title
cost, cost-effectiveness and cost utility
Description
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.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Francois Pattou, Professor
Phone
00 33 3 20 44 42 73
Email
fpattou@iv-lille2.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francois Pattou, Professor
Organizational Affiliation
University Hospital of Lille
Official's Role
Study Director
Facility Information:
Facility Name
University Hospital of Lille
City
Lille
State/Province
Nord
ZIP/Postal Code
59000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Violeta Raverdy, MD
Phone
00 33 3 20 44 59 62
Email
vraverdi@univ-lille2.fr
First Name & Middle Initial & Last Name & Degree
Pierre Fontaine, Professor
Facility Name
Centre Hospitalier Regional D' Angers
City
Angers
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vincent Romher, MD,PhD
Facility Name
Hopital de Bois-Guillaume Chu Rouen
City
Bois-Guillaume
Country
France
Individual Site Status
Recruiting
Facility Name
Hu Ouest Site Ambroise Pare Aphp -
City
Boulogne-Billancourt
Country
France
Individual Site Status
Recruiting
Facility Name
Hopital Jeanne D'Arc Chu Nancy
City
Dommartin Les Toul
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Didier Quillot, MD,PhD
Facility Name
Hopital Lyon Sud - Hcl - Pierre Benite
City
Lyon
ZIP/Postal Code
69008
Country
France
Individual Site Status
Recruiting
Facility Name
Hopital Lapeyronie Chu Montpellier
City
Montpellier
Country
France
Individual Site Status
Recruiting
Facility Name
Hu Pitie Salpetriere Aphp
City
Paris
Country
France
Individual Site Status
Recruiting
Facility Name
Hopital Larrey Chu Toulouse
City
Toulouse
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick RITZ, MD,PhD
Facility Name
Ch Valenciennes
City
Valenciennes
Country
France
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparison of Gastric By-Pass and Optimized Medical Treatment in Obese Diabetic Patients

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