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Terminated Not applicable Interventional

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

ClinicalTrials.gov ID: NCT00200044

Public ClinicalTrials.gov record NCT00200044. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 4:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Gatekeeper® System Sham-Controlled Study for the Treatment of GERD

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00200044
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
MedtronicNeuro
Industry
Enrollment
143 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2002 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Jun 2008 (Actual)
Last update posted
Jul 13, 2009

2002 – 2008

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
Contact Medtronic for specific site information San Francisco California 94115 —
Contact Medtronic for specific site information Atlanta Georgia 30322 —
Contact Medtronic for specific site information Chicago Illinois 60611 —
Contact Medtronic for specific site information Indianapolis Indiana 46202 —
Contact Medtronic for specific site information Lexington Kentucky 40536 —
Contact Medtronic for specific site information St Louis Missouri 63110 —
Contact Medtronic for specific site information Lebanon New Hampshire 03756 —
Contact Medtronic for specific site information New York New York 10021 —
Contact Medtronic for specific site information Knoxville Tennessee 37909 —
Contact Medtronic for specific site information Milwaukee Wisconsin 53233 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00200044, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 13, 2009 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00200044 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →