Clinical trial
A Post-Approval Study of the LINX® Reflux Management System
NCT01940185 · Torax Medical Incorporated, Industry · Completed
Key facts
| NCT number | NCT01940185 |
|---|---|
| Title | A Post-Approval Study of the LINX® Reflux Management System |
| Official title | A Post-Approval Study of the LINX® Reflux Management System |
| Lead sponsor | Torax Medical Incorporated, Industry |
| Status | Completed |
| Study type | Observational |
| Conditions | Gastroesophageal Reflux Disease (GERD) |
| Intervention type | Device |
| Interventions | LINX device |
| Enrollment | 200 |
| Start date | Jun 30, 2012 |
| Primary completion | Jun 30, 2023 |
| Completion | Jun 30, 2023 |
| First posted | Sep 12, 2013 |
| Last update posted | Jan 5, 2024 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No Results posted
- 1–9 Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: