Trials / Unknown
UnknownNCT02227771
Consistent CTO Trial
CONventional Antegrade vs Sub-Intimal Synergy sTENTing in Chronic Total Occlusions
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 215 (estimated)
- Sponsor
- European Cardiovascular Research Center · Network
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to demonstrate that enhanced vascular healing with the Synergy stent should minimize the risk of late aneurysm formation and potential clinical complications but not at the cost of enhanced efficacy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Percutaneous coronary intervention |
Timeline
- Start date
- 2014-12-01
- Primary completion
- 2016-12-31
- Completion
- 2018-12-01
- First posted
- 2014-08-28
- Last updated
- 2017-05-18
Locations
6 sites across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT02227771. Inclusion in this directory is not an endorsement.