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临床试验/NCT01035333
NCT01035333已完成4 期

A Pilot Study of the Efficacy of Alli in the Management of Pre-operative Weight Loss Required for Bariatric Surgery.

Albany College of Pharmacy and Health Sciences1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2009年11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
已完成
入组人数
19
试验地点
1
主要终点
Weight Loss

研究概览

简要总结

The primary goal of the study is to determine if orlistat 60mg (Alli) is effective in helping patients achieve a required 10% weight loss goal prior to bariatric surgery. The medication will be added to the usual standard of care which includes education regarding diet and exercise and monthly meetings with a registered dietician.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • adult patients preparing for gastric bypass surgery

排除标准

  • pregnancy

研究组 & 干预措施

orlistat 60mg

Experimental

Patients assigned to treatment group for up to 6 months of therapy.

干预措施: Orlistat (Drug)

结局指标

主要结局

Weight Loss

时间窗: 6 months

Weight loss acheived during time on study up to 6 months.

次要结局

  • Patient Satisfaction(6 months)

研究者

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

Margaret Malone

Dr

Albany College of Pharmacy and Health Sciences

研究点 (1)

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