Trial record 18 of 44 for:    Open Studies | "Body Mass Index"

Laparoscopic Gastric Bypass for Type 2 Diabetes Mellitus With Body Mass Index (BMI) < 35

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2011 by Weill Medical College of Cornell University.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Weill Medical College of Cornell University
ClinicalTrials.gov Identifier:
NCT00999050
First received: October 14, 2009
Last updated: January 3, 2011
Last verified: January 2011
  Purpose

The aim of this study is to evaluate the effect of Roux-en-y gastric bypass (RYGB) in controlling diabetes in subjects with mild obesity (BMI 26-35). The primary endpoint will be the reduction of HbA1c (< 7%), a standard measure of diabetes control; the secondary endpoints will be changes blood sugar , vitamin levels, insulin, c-peptide, and lipids levels, as well as retinal eye examinations, urinalysis to assess kidney function, carotid ultrasound as a marker of cardiovascular function, and alterations in diabetic medications. Fifty subjects with medically documented type 2 Diabetes Mellitus (T2DM) with BMIs between 26 and 35 will undergo standard laparoscopic RYGB. Prior and after surgery, the subjects will undergo a clinical evaluation in regard to the primary and secondary endpoints listed. The pre-surgery evaluation is directed toward establishing the existence of diabetes related complications prior to surgery. After surgery subjects will be closely monitored for complications and required changes in their diabetes management. Repeat assessments will be made at 1, 3, 6, and 12 months and at two years.


Condition Intervention
Diabetes Mellitus, Type 2
Procedure: Gastric bypass for diabetic patients <35 BMI

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Laparoscopic Gastric Bypass for Type 2 Diabetes Mellitus: a Pilot Prospective Study in Overweight and Mildly Obese Subjects

Resource links provided by NLM:


Further study details as provided by Weill Medical College of Cornell University:

Primary Outcome Measures:
  • Hemoglobin A1C changes [ Time Frame: Post gastric bypass operation ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • improvement in glycemic control [ Time Frame: 1 to two years ] [ Designated as safety issue: No ]

Estimated Enrollment: 50
Study Start Date: October 2009
Estimated Study Completion Date: November 2013
Estimated Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: diabetic pts <35BMI
All patients will be in a single arm receiving bypass surgery to assist with diabetes management
Procedure: Gastric bypass for diabetic patients <35 BMI
The operation is performed under general anesthesia. It is done laparoscopically, meaning that several small openings are made in the abdomen for insertion of long, thin surgical instruments, one with an attached camera. The operation is video monitored. The top of the stomach is divided across, leaving a small pouch for food. The rest of the stomach remains but can receive no food. The gut is divided just past the stomach, and it is attached to the small stomach pouch so that food can get back into the bowel. A second connection is made so that the bile and digestive juices pass into the bowel with the food.
Other Name: gastric bypass surgery

Detailed Description:

The primary endpoint will be the reduction of HbA1c and secondary endpoints will be multiple associated parameters as listed below. A group of 50 subjects with medically documented T2DM and BMI of 26-35 will undergo standard laparoscopic RYGB. Prior to surgery, the subjects will undergo the standard pre-operative work up required for conventional bariatric surgery. This includes full history and physical exam, medical/cardiac clearances as needed, nutrition consultation and a gastrointestinal consultation for upper endoscopy. After thorough explanation an approved informed consent will be signed. Baseline parameters, as listed below, will be measured for each subject to identify possible complications of diabetes prior to the surgical intervention..

After surgery perioperative complications will be monitored and required modifications of diabetes management advised. Followed up measurements at 1, 3, 6, 12, and 24 months is consistent with standard clinical practice guidelines. Data analysis will be ongoing to observe the effects of the surgical intervention on glucose homeostasis.

  • Baseline parameters
  • History and Physical Exam
  • Weight/BMI/ body composition with the Tanita 310.
  • Waist Circumference
  • Blood Pressure
  • CBC
  • HbA1c
  • Fasting glucose
  • Vitamin B6, B12, Folate,and Iron status
  • Lipid Profile -total cholesterol, HDL, LDL, triglyceride
  • Fasting Insulin and C-peptide
  • Stimulated C-peptide
  • EKG
  • Retinal exam
  • Urinalysis (assess for proteinuria and microalbuminuria)
  • Comprehensive foot exam
  • Medications and dosage
  • Quality of Life Score (SF-36)
  • Carotid ultrasound (intima-media thickness)

Follow-up:

4 Weeks:

  • Physical Examination, wound check, Body weight, BMI,
  • Glucose Diary (pre and postprandial glucose levels as required)
  • Insulin and C-peptide
  • Lipid profile
  • Medication use

    3 Months, 6 months,

Same as above plus:

  • HbA1c
  • Vitamin levels and iron status
  • Retinal exam
  • Annually the baseline measurements will be repeated
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Adult males and females who meet the following inclusion criteria will be offered the opportunity to participate in the study:

  1. Diagnosis of type 2 Diabetes Mellitus (T2DM) confirmed by the following criteria:

    1. normal or high C-peptide level (> 0.9 ng/ml) to exclude type 1 Diabetes Mellitus
    2. positive glucagon test to confirm T2DM
    3. fasting plasma glucose of 126 mg/dl or more on at least two occasions
  2. Body mass index (BMI) 26 kg/m2 or greater, and less than 35 kg/m2
  3. History of T2DM for not longer than 8 years, as long-standing disease beyond 8 years correlates with failure to achieve diabetes resolution after gastric bypass
  4. No contraindication for surgery or general anesthesia as determined by a multidisciplinary bariatric surgery team (surgeon, anesthesiologist, internist, dietitian, psychologist)
  5. Between 18 and 65 year of age
  6. Able to provide informed consent
  7. If a female with reproductive potential, she has to agree to use a reliable method of birth control for at least one year from the date of surgery

Exclusion Criteria

Subjects who meet any of the following exclusion criteria will not be eligible to participate in the study:

  1. Enrollment in another clinical study, which involves an investigational drug
  2. Diagnosis of type 1 Diabetes Mellitus or other genetic forms of Diabetes Mellitus
  3. Significant renal failure of chronic liver disease (except NAFLD)
  4. Major psychological disorders
  5. Pregnancy - all female subjects will have serum beta-hCG prior to operation, and must use birth control of their choice to avoid pregnancy during the first year after surgery
  6. Previous gastric or esophageal surgery
  7. Immunosuppressive drugs including corticosteroids
  8. Coagulopathy defined as an INR > 1.5 or platelet count < 50,000/µl
  9. Anemia defined as a Hb <10.0 g/dl
  10. Inflammatory bowel diseases or other medical condition that would serve as a contraindication to gastric bypass (eg. celiac sprue, pancreatic insufficiency)
  11. A severe concurrent illness that is likely to limit life or require extensive systemic treatment (e.g. cancer)
  12. A pre-existing major complication of diabetes:

    1. unstable, proliferative retinopathy
    2. severe autonomic cardiac neuropathy or intestinal neuropathy
    3. Myocardial infarction within the previous year, current unstable angina, or poorly-controlled congestive heart failure (Stage III)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00999050

Contacts
Contact: Maureen Morrison, MSN-ACNP, DNPc 212-746-5925 msm7003@med.cornell.edu
Contact: Tina Chuck, MPH 212-746-5725 tic2005@med.cornell.edu

Locations
United States, New York
Weill Cornell Medical College New York Prysbyterian Hosptial Recruiting
New York, New York, United States, 10065
Contact: Francisco Rubino, MD    212-746-5925    frr2007@med.cornell.edu   
Contact: Gladys W Strain, PhD    212-746-5661    gls2010@med.cornell.edu   
Sponsors and Collaborators
Weill Medical College of Cornell University
  More Information

Publications:
Responsible Party: Francesco Rubino, MD, Assistant Professor, Weill Medical College
ClinicalTrials.gov Identifier: NCT00999050     History of Changes
Other Study ID Numbers: 0906010450
Study First Received: October 14, 2009
Last Updated: January 3, 2011
Health Authority: United States: Institutional Review Board

Keywords provided by Weill Medical College of Cornell University:
type two diabetes
gastric bypass surgery
overweight or moderately obese

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases

ClinicalTrials.gov processed this record on October 19, 2014