Gatekeeper European 005

Stopped early

Conditions studied: GERD

In brief

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

Key facts

Study ID

NCT00229086

Run by

MedtronicNeuro

People needed

55

Last updated by the study team

2008-07-28

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must have been part of the Endo 2000-03 or Endo 2000-04 clinical study
• Subjects who have been informed of the nature of the long-term follow-up study and have agreed to its participation and provided Informed Consent

You may not qualify if…

• Underwent another endoscopic or surgical treatment for GERD (except re-intervention with Gatekeeper)
• Developed other medical illness that may cause the subject to be non-compliant
• Extensive Barrett's Esophagus (>2 cm)
• Unable or unwilling to cooperate with the study procedures

Where it is running

• Contact Medtronic for specific site information — Minneapolis, Minnesota, United States
• Contact Medtronic for specific location — Tolochenaz, Switzerland

Full record on ClinicalTrials.gov

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