Gatekeeper European 005
NCT00229086 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 55
Last updated 2008-07-28
Summary
Evaluation of the Gatekeeper System in the treatment of patients with Gastroesophageal Reflux Disease (GERD) who already have been treated under study protocols Endo 2000-03 and Endo 2000-04
Conditions
- GERD
Interventions
- DEVICE
-
Gatekeeper Reflux Repari System (Device)
Sponsors & Collaborators
-
MedtronicNeuro
lead INDUSTRY
Principal Investigators
-
Medtronic GU Investigator · MedtronicNeuro
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- United States
- Switzerland
Study Locations
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