Gatekeeper European 005

NCT00229086 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 55

Last updated 2008-07-28

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00229086 on ClinicalTrials.gov