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临床试验/NCT00584389
NCT00584389终止4 期

The Effect of Rimonabant on Energy Expenditure, Fat Metabolism and Body Composition

University of Surrey1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2007年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
14
试验地点
1
主要终点
The direct effect of rimonabant on energy expenditure

研究概览

简要总结

This study will determine in obese subjects the direct effects of the weight loss drug rimonabant (ie independent of weight loss) on energy expenditure, fat metabolism and and body fat distribution. We hypothesise that rimonabant will increase energy expenditure. The fuel for the increased energy expenditure will come from fat. As a result of burning more fat there will be a decrease in fat in blood and an improvement in the body's response to insulin.

详细描述

In obese subjects (BMI 33-38kg/m2) completing 12 months of treatment with the CB1 antagonist rimonabant (SR141716) there was an average weight loss from baseline of approximately 8.5 kg. These studies also showed the weight loss was accompanied by a decrease in plasma triglyceride (TG), an increase in HDL cholesterol and an improvement in insulin sensitivity measured by HOMA-IR. When adjusted for weight loss 50% of the improvements in TG, HDL cholesterol, and insulin sensitivity was not attributable to weight loss. This suggests that rimonabant has direct effects on fat metabolism.

This study will investigate the direct effects of rimonabant (ie independent of weight loss) in a 2 group randomised study. One group will receive rimonabant for 12 weeks and the other group will have a dietary intervention to match the weight loss in the rimonabant group. Measurements of energy expenditure (using indirect calorimetry and Actiheart monitors),fatty acid and triglyceride metabolism (using stable isotope techniques) and body fat distribution (by magnetic resonance imaging) will be made before and after the intervention. To determine the possible mechanisms of the changes in metabolism, gene expression of key regulators of fatty acid metabolism in adipose and muscle tissue and circulating levels of adipokines will be measured.

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
50 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Healthy Caucasian postmenopausal women
  • BMI 30-38

排除标准

  • Not currently weight-stable
  • Diagnosed with diabetes
  • Cardiovascular disease
  • Endocrine disease
  • Hepatic and renal disorders
  • Neurological/psychological illness/history of depression
  • Previous surgical procedures for weight loss
  • Medications known to alter body weight or appetite
  • β-blockers, fibrates and metformin
  • Severe under-reporting of food intake based on a 4 day food diary

研究组 & 干预措施

1

Experimental

Rimonabant treatment (20mg/d) for 12 weeks

干预措施: rimonabant (Drug)

2

Other

Dietary intervention

干预措施: Dietary intervention (Behavioral)

结局指标

主要结局

The direct effect of rimonabant on energy expenditure

时间窗: 12 weeks

次要结局

  • Whole body fatty acid production and oxidation rate.(12 weeks)
  • Triglyceride synthesis and clearance rate.(12 weeks)
  • Whole body fat distribution.(12 weeks)
  • Adipose tissue and muscle mRNA levels of key regulators of fatty acid metabolism.(12 weeks)
  • Insulin sensitivity.(12 weeks)

研究者

申办方类型
Other

研究点 (1)

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