An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS With Gastroesophageal Reflux Disease (GERD)
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.
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
- Enrollment
- 143 participants
Conditions and interventions
Conditions
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
- Nov 30, 2002
- Primary completion
- May 31, 2006
- Completion
- May 31, 2008
- Last update posted
- Jul 12, 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 12, 2009 · Synced Sep 1, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00200044 live on ClinicalTrials.gov.