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临床试验/NCT00469391
NCT00469391已完成2 期

A Multi-Center, Pilot Efficacy Study of the GI Sleeve for Pre-Surgical Weight Loss

Morphic Medical Inc.8 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2007年6月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
56
试验地点
8
主要终点
Percent Excess Weight Loss (%EWL) at Week 12

研究概览

简要总结

The purpose of the study is to evaluate the safety and efficacy of the GI Sleeve in patients who require weight loss prior to their Bariatric surgery.

详细描述

This is a randomized, patient blinded, prospective study.Patients will receive either a device or a sham procedure. Patients will be evaluated for the study and randomized to a treatment group if they qualify for the study. Throughout the study their weights will be obtained and various laboratory tests collected. A comparison of weight loss between the two groups will be assessed as the primary outcome measure.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • BMI > 35 with a significant comorbid condition or BMI 40-60
  • Candidate for Bariatric Surgery

排除标准

  • No pathologies of the GI Tract
  • No anti-coagulant or non-steroidal anti-inflammatory medications

结局指标

主要结局

Percent Excess Weight Loss (%EWL) at Week 12

时间窗: 3 months

Excess Weight Loss was calculated using the Metropolitan Life Table (MET method)

次要结局

未报告次要终点

研究者

发起方
Morphic Medical Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (8)

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