Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the Treatment of Type 2 Diabetes
Status: | Completed |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 21 - 65 |
Updated: | 4/2/2016 |
Start Date: | October 2010 |
End Date: | October 2014 |
Contact: | Melissa Marine |
Email: | mem9065@med.cornell.edu |
Phone: | 212-746-5725 |
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
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.
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.
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
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