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OpenTrials
Completed

NCT Number: NCT01288456

Study to Evaluate Novel Gastric Space Occupying Device

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.

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Key information

Age range

21 year–64 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Obesity Control Center

Tijuana, Estado de Baja California, Mexico

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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;

Sponsors and collaborators

Lead sponsor

Obalon Therapeutics, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Feb 2, 2011
Registry last updated
May 28, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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