Clinical trial
BIOHELIX-I Bare Metal Stent Study
NCT01612767 · Biotronik, Inc., Industry · Completed
Key facts
| NCT number | NCT01612767 |
|---|---|
| Title | BIOHELIX-I Bare Metal Stent Study |
| Official title | The Treatment of Coronary Artery Lesions Using the PRO-Kinetic Energy Cobalt-Chromium, Bare-Metal Stent |
| Acronym | BIOHELIX-I |
| Lead sponsor | Biotronik, Inc., Industry |
| Status | Completed |
| Phase | Phase 2/Phase 3 |
| Study type | Interventional |
| Conditions | Coronary Arteries Disease |
| Intervention type | Device |
| Interventions | PRO-Kinetic Energy Stent |
| Enrollment | 329 |
| Start date | Nov 1, 2012 |
| Primary completion | Sep 1, 2015 |
| Completion | Nov 1, 2017 |
| First posted | Jun 6, 2012 |
| Last update posted | Sep 28, 2018 |
| Countries | Colombia, Germany, Latvia, Netherlands, United States |
At a glance
- Yes 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: