Trials / Terminated
TerminatedNCT01811927
The Treatment of Coronary Artery Lesions Using the PRO-Kinetic Energy Cobalt-Chromium, Bare-Metal Stent
The Treatment of Coronary Artery Lesions Using the PRO-Kinetic Energy Cobalt-Chromium, Bare-Metal Stent (BIOHELIX-II)
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 43 (actual)
- Sponsor
- Biotronik AG · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to the assess the clinical performance of the BIOTRONIK PRO-Kinetic Energy stent in subjects with atherosclerotic disease of native coronary arteries.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PRO-Kinetic Energy Stent | Bare-metal stent |
Timeline
- Start date
- 2013-03-01
- Primary completion
- 2014-10-01
- Completion
- 2014-10-01
- First posted
- 2013-03-15
- Last updated
- 2015-03-24
Locations
3 sites across 2 countries: Netherlands, Switzerland
Source: ClinicalTrials.gov record NCT01811927. Inclusion in this directory is not an endorsement.