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临床试验/NCT01288456
NCT01288456已完成不适用

A Single Centre 30-day Observational Non-randomised Study to Evaluate Preliminary Safety and Efficacy of a Novel Gastric Space Occupying Device as an Aid for Weight Loss

Obalon Therapeutics, Inc.1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1

研究概览

简要总结

This will be an observational, prospective, non-randomized, pilot study to gain initial device experience on a novel space-occupying device in persons who are overweight or obese. No formal hypothesis testing will be conducted.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
21 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 21-64 years
  • BMI 27-40 Kg/m2
  • No history of weight reduction of more than 5% of total body weight in the past 6 months

排除标准

  • Have unstable angina, myocardial infarction within the past year, or heart disease classified within the New York Heart Association's Class III or IV functional capacity;
  • Be taking chronic aspirin or other non steroidal anti-inflammatory agents, or other medications known to be gastric irritants, and unwillingness to discontinue the use of these concomitant medications, antiarrythmics, anti-anginal medications, anticoagulants or medications for congestive heart failure;
  • Be taking blood pressure medications, unless their blood pressure is controlled and they have been at stable dose for at least 3 months;
  • Have type 1 diabetes or type 2 diabetes requiring oral medications or insulin;
  • History or symptoms of thyroid disease which is not controlled by medication;
  • Have severe renal, hepatic, pulmonary disease or cancer;
  • Past history of gastrointestinal surgery (excluding uncomplicated appendectomy);
  • Have a history of adhesive peritonitis;
  • History or symptoms of esophageal and/or gastric varices;
  • Have history or congenital or acquired GI anomalies (e.g. atresias, stricture, and /or diverticula);
  • History or symptoms of inflammatory bowel disease, such as Chron's disease;
  • History of/ signs and /or symptoms of duodenal or gastric ulcer;
  • Have gastroparesis;
  • Pregnant or breastfeeding or intention of becoming pregnant during the study (if female of childbearing potential);
  • Currently using pharmaceutical agents for weight loss;

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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