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临床试验/NCT01763346
NCT01763346已完成不适用

Beta Cell Restoration Through Fat Mitigation

University of Southern California1 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2013年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
88
试验地点
1
主要终点
Steady State Beta Cell Compensation

研究概览

简要总结

Weight loss achieved through gastric banding will be superior to treatment with metformin in preserving or restoring pancreatic beta cell function in people with prediabetes or mild type 2 diabetes.

详细描述

BetaFat is a 2-arm, unblinded study to compare gastric banding to treatment with metformin over a 24-month period in moderately obese adults with pre- or mild type 2 diabetes. The primary outcome will be change in β-cell compensation for insulin resistance, which the investigators will compare between groups. Secondary analyses will include other potential markers of β-cell health and potential mediators of treatment-specific effects. The main focus will be on mediators related to obesity. Clinically, the project will serve as a test of concept for use of gastric banding relatively early in the spectrum of obesity and β-cell disease. Biologically, the results will provide crucial information on potential mediators of β-cell failure and its arrest or reversal in the context of obesity. Those mediators will guide the development of more effective treatment and monitoring for the β-cell disease that causes type 2 diabetes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
22 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Prior completion of at least two months in a diet, exercise and lifestyle intervention program within the past two years
  • Fasting plasma glucose >90 mg/dl plus 2-hour glucose ≥140 mg/dl on 75 gm OGTT plus HbA1C ≤7.0%. There is no lower limit for the A1C and no upper limit for the OGTT 2-hour glucose based on prior studies that allow us to identify people with falling β-cell function
  • Age 22-65 years
  • Body mass index (BMI) 30-40 kg/m2
  • For participants with diabetes, known duration <1 year
  • No history of use of antidiabetic medications except during pregnancy

排除标准

  • Contraindications to LapBand(see Appendix 1)
  • Contraindication to MRI (claustrophobia; permanent metal objects such as pacemakers, prostheses, aneurysm clips)
  • Underlying disease(s) likely to (a) limit life span to less than study duration and/or (b) increase risk of intervention outside of the study and/or (c) limit ability to participate in outcomes assessment and/or (d) limit participation
  • An underlying disease known to have important effects on glucose metabolism
  • Active infections
  • Renal disease (serum creatinine ≥1.4 mg/dl for men; ≥1.3 mg/dl for women) or serum potassium abnormality (<3.4 or >5.5 mmol/l)
  • Anemia (hemoglobin <11g/dl in women, <12 g/dl in men) or known coagulopathy
  • Cardiovascular disease, including uncontrolled hypertension and symptomatic congestive heart failure. Participants must be able to safely tolerate administration of fluid/volume challenges during clamp studies.
  • Serum AST >3 times upper limit of normal in local clinical lab
  • Excessive alcohol intake
  • Suboptimally treated thyroid disease
  • Conditions or behaviors likely to affect the conduct of the study
  • unable or unwilling to give informed consent
  • unable to adequately communicate with clinic staff
  • another household member is a participant or staff member
  • current or anticipated participation in another intervention research project that would interfere with any of the interventions/outcomes
  • likely to move away from participating clinic in next 2 years
  • current (or anticipated) pregnancy and lactation.
  • major psychiatric disorder that, in the opinion of clinic staff, would impede the conduct of the study
  • weight loss >5% in past three months for any reason except postpartum weight loss.
  • additional conditions may serve as criteria for exclusion at the discretion of the local site

研究组 & 干预措施

metformin

Active Comparator

subjects receiving metformin

干预措施: Metformin (Drug)

gastric banding

Experimental

subjects receiving LAP-BAND

干预措施: gastric banding (Device)

结局指标

主要结局

Steady State Beta Cell Compensation

时间窗: 24 months

mean plasma C-peptide concentration during clamp steady state, adjusted for mean clamp insulin sensitivity

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Buchanan

Professor

University of Southern California

研究点 (1)

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