An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS With Gastroesophageal Reflux Disease (GERD)

Stopped early · Not applicable · Has a placebo group

Conditions studied: Gastroesophageal Reflux Disease

In brief

The purpose of the study is to demonstrate the intended use of the Gatekeeper Reflux Repair System to provide symptomatic relief is subjects with gastroesophageal reflux disease.

Key facts

Study ID

NCT00200044

Run by

MedtronicNeuro

People needed

143

Starts

2002-12-01

Expected to finish

2008-06-01

Last updated by the study team

2009-07-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Contact Medtronic for specific site information — San Francisco, California, United States
• Contact Medtronic for specific site information — Atlanta, Georgia, United States
• Contact Medtronic for specific site information — Chicago, Illinois, United States
• Contact Medtronic for specific site information — Indianapolis, Indiana, United States
• Contact Medtronic for specific site information — Lexington, Kentucky, United States
• Contact Medtronic for specific site information — St Louis, Missouri, United States
• Contact Medtronic for specific site information — Lebanon, New Hampshire, United States
• Contact Medtronic for specific site information — New York, New York, United States
• Contact Medtronic for specific site information — Knoxville, Tennessee, United States
• Contact Medtronic for specific site information — Milwaukee, Wisconsin, United States
• Contact Medtronic for specific site information — Amsterdam, Netherlands

Full record on ClinicalTrials.gov

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