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Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the Treatment of Type 2 Diabetes

Primary Purpose

Type 2 Diabetes

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Roux-en-Y-Gastric Bypass
Intensive lifestyle modification and Optimal medical Therapy
Sponsored by
Weill Medical College of Cornell University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes

Eligibility Criteria

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

Inclusion Criteria:

  1. Diagnosed with type 2 diabetes by any of the following:

    • A fasting plasma glucose > 126 mg/dl confirmed on repeated testing
    • 2 hour plasma glucose > 200mg/dl during a 75 gram oral glucose tolerance test
    • HbA1c >6.5%
  2. A normal or high C-peptide level (> 0.9 ng/ml) to exclude type 1 diabetes and insulin deficient type 2 diabetes
  3. Negative AntiGAD 65 Antibodies
  4. Body mass index (BMI) between 28 and 35 kg/m2 ( > 27.6 kg/m2 and < 34.5 kg/m2 ) that reflect a condition of overweight to moderate obesity.

    In consideration of the evidence that the associations between BMI, percentage of body fat, and CV risk differ across populations, and that the proportion of Asian people with a high risk of type 2 diabetes and cardiovascular disease is substantial at BMI's lower than the existing WHO cut-off point for overweight (= 25 kg/m2) (source: WHO Expert consultation. Lancet. 2004 Jan 10;363(9403):157-63), the lower BMI cut-off for inclusion in this study will be 26kg/m2 for patients of Asian descent.

  5. No contraindications for surgery or General Anesthesia as determined by a multidisciplinary team (surgeon, endocrinologist/internist, cardiologist, nutritionist)
  6. . Between 21 and 65 years of age
  7. . Able to provide informed consent
  8. . If a female with reproductive potential, agreement to use a reliable method of birth control for 2 years following surgery (Barrier, birth control, patch).

    This precaution is necessary to prevent potential complications of pregnancy due to possible nutritional deficiencies in the period of more intense weight loss after surgery. On the other hand, this precaution will avoid erratic weight/glucose tolerance changes of pregnancy effecting results.

  9. Have valid health insurance

Exclusion Criteria:

  1. Diagnosis of diabetes more than 15 years (to exclude pts with significant decline in pancreatic function from long-standing diabetes)
  2. Insulin therapy for more than 12 years
  3. HbA1c higher than 10%
  4. Diagnosis of type 1 diabetes
  5. Enrolled in another clinical study which involves an investigational drug
  6. Major psychological disorders
  7. Pregnancy (all female patients will have serum beta hCG) or planned pregnancy within two years of entry into the study or unwilling to use reliable contraceptive method
  8. Previous gastric or esophageal surgery
  9. Immunosuppressive drugs including corticosteroids
  10. Coagulopathy (INR > 1.5 or platelets < 50,000/μl)
  11. Anemia (Hb < 10.0 g/dl)
  12. Any contraindication to laparoscopic gastric bypass or medical diabetes therapy
  13. A severe concurrent illness likely to limit life (e.g. cancer) or requiring extensive systemic treatment (e.g. ulcerative colitis)
  14. A significant malabsorptive or gastrointestinal disorder (e.g. pancreatic insufficiency, Celiac sprue, or Crohn's disease)
  15. Significant proteinuria (> 250 mg/dl)
  16. Severe neuropathy or clinical diagnosis of gastropathy (early satiety, nausea, vomiting, constipation alternating with diarrhea)
  17. Myocardial infarction in the previous year, current angina or heart failure

Sites / Locations

  • Weill Cornell Medical CollegeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Lifestyle modification

Roux-en-Y-Gastric Bypass

Arm Description

Intensive nutritional/exercise counseling for weight loss by lifestyle modification in addition to optimum medical treatment.

A laparoscopic gastric bypass will be performed in the treatment of type 2 diabetes in Overweight-to-Moderately Obese Patients

Outcomes

Primary Outcome Measures

The primary end-point will be the control of hyperglycemia (HbA1c <6.5% + FG<126mg/dl).

Secondary Outcome Measures

Short (2 yrs) and long term (5 yrs.) achievement of 'adequate" glycemic control, mean change in HbA1c from baseline.

Full Information

First Posted
October 27, 2010
Last Updated
December 20, 2012
Sponsor
Weill Medical College of Cornell University
Collaborators
Medtronic - MITG
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1. Study Identification

Unique Protocol Identification Number
NCT01231308
Brief Title
Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the Treatment of Type 2 Diabetes
Official Title
Roux-en-Y-Gastric Bypass (RYGB) Versus Lifestyle Modification Plus Medical Therapy in the Treatment of Type 2 Diabetes in Overweight-to-Moderately Obese Patients: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Unknown status
Study Start Date
October 2010 (undefined)
Primary Completion Date
October 2013 (Anticipated)
Study Completion Date
October 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Weill Medical College of Cornell University
Collaborators
Medtronic - MITG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study is aimed to compare: Laparoscopic Roux-en-Y-Gastric Bypass (RYGB) + optimal medical therapy versus Intensive lifestyle modification and optimal medical therapy in the treatment of type 2 diabetes in overweight-to-moderately obese patients (BMI: 28-34kg/m2; the lower BMI cut-off will be 26kg/m2 in patients of Asian descent). This is a single center, prospective randomized study. The study at the Weill College Medical College Diabetes Surgery Center. This study is intended to be a pilot investigation whose results can inform clinicians and researchers for future larger or multi-site trials of diabetes surgery. This study will also be used for the definition of a "core" protocol for independent randomized clinical trials to be carried out at various centers participating in a multinational consortium.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lifestyle modification
Arm Type
Active Comparator
Arm Description
Intensive nutritional/exercise counseling for weight loss by lifestyle modification in addition to optimum medical treatment.
Arm Title
Roux-en-Y-Gastric Bypass
Arm Type
Experimental
Arm Description
A laparoscopic gastric bypass will be performed in the treatment of type 2 diabetes in Overweight-to-Moderately Obese Patients
Intervention Type
Procedure
Intervention Name(s)
Roux-en-Y-Gastric Bypass
Intervention Description
Standard laparoscopic gastric bypass. Preoperative preparation will include antibiotic prophylaxis given less than 60 minutes prior to making the first incision. Under general anesthesia with endotracheal intubation, a laparoscopic gastric bypass will be performed in the usual fashion.
Intervention Type
Behavioral
Intervention Name(s)
Intensive lifestyle modification and Optimal medical Therapy
Intervention Description
Very low calorie diet consisting of 5 feedings: 2 liquid meal replacements, 2 low-calorie snacks, and 1 small meal of known caloric content. After 10% weight loss is achieved, the subjects will received individualized nutrition sessions beginning bi-weekly but extending time intervals as the weight loss progresses.
Primary Outcome Measure Information:
Title
The primary end-point will be the control of hyperglycemia (HbA1c <6.5% + FG<126mg/dl).
Time Frame
Monthly after initiation of study for a minimum of 3 months, and then every monthly until HbA1c is below 7%
Secondary Outcome Measure Information:
Title
Short (2 yrs) and long term (5 yrs.) achievement of 'adequate" glycemic control, mean change in HbA1c from baseline.
Time Frame
Year 2 and year 5

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with type 2 diabetes by any of the following: A fasting plasma glucose > 126 mg/dl confirmed on repeated testing 2 hour plasma glucose > 200mg/dl during a 75 gram oral glucose tolerance test HbA1c >6.5% A normal or high C-peptide level (> 0.9 ng/ml) to exclude type 1 diabetes and insulin deficient type 2 diabetes Negative AntiGAD 65 Antibodies Body mass index (BMI) between 28 and 35 kg/m2 ( > 27.6 kg/m2 and < 34.5 kg/m2 ) that reflect a condition of overweight to moderate obesity. In consideration of the evidence that the associations between BMI, percentage of body fat, and CV risk differ across populations, and that the proportion of Asian people with a high risk of type 2 diabetes and cardiovascular disease is substantial at BMI's lower than the existing WHO cut-off point for overweight (= 25 kg/m2) (source: WHO Expert consultation. Lancet. 2004 Jan 10;363(9403):157-63), the lower BMI cut-off for inclusion in this study will be 26kg/m2 for patients of Asian descent. No contraindications for surgery or General Anesthesia as determined by a multidisciplinary team (surgeon, endocrinologist/internist, cardiologist, nutritionist) . Between 21 and 65 years of age . Able to provide informed consent . If a female with reproductive potential, agreement to use a reliable method of birth control for 2 years following surgery (Barrier, birth control, patch). This precaution is necessary to prevent potential complications of pregnancy due to possible nutritional deficiencies in the period of more intense weight loss after surgery. On the other hand, this precaution will avoid erratic weight/glucose tolerance changes of pregnancy effecting results. Have valid health insurance Exclusion Criteria: Diagnosis of diabetes more than 15 years (to exclude pts with significant decline in pancreatic function from long-standing diabetes) Insulin therapy for more than 12 years HbA1c higher than 10% Diagnosis of type 1 diabetes Enrolled in another clinical study which involves an investigational drug Major psychological disorders Pregnancy (all female patients will have serum beta hCG) or planned pregnancy within two years of entry into the study or unwilling to use reliable contraceptive method Previous gastric or esophageal surgery Immunosuppressive drugs including corticosteroids Coagulopathy (INR > 1.5 or platelets < 50,000/μl) Anemia (Hb < 10.0 g/dl) Any contraindication to laparoscopic gastric bypass or medical diabetes therapy A severe concurrent illness likely to limit life (e.g. cancer) or requiring extensive systemic treatment (e.g. ulcerative colitis) A significant malabsorptive or gastrointestinal disorder (e.g. pancreatic insufficiency, Celiac sprue, or Crohn's disease) Significant proteinuria (> 250 mg/dl) Severe neuropathy or clinical diagnosis of gastropathy (early satiety, nausea, vomiting, constipation alternating with diarrhea) Myocardial infarction in the previous year, current angina or heart failure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Melissa Marine
Phone
212-746-5725
Email
mem9065@med.cornell.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesco Rubino, MD
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Weill Cornell Medical College
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melissa Marine
Phone
212-746-5725
Email
mem9065@med.cornell.edu
First Name & Middle Initial & Last Name & Degree
Francesco Rubino, MD

12. IPD Sharing Statement

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Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the Treatment of Type 2 Diabetes

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