Trials / Terminated
TerminatedNCT02622100
Evaluation of Effectiveness and Safety of Bioresorbable Vascular Scaffold in Routine Clinical Practice
Evaluation of Effectiveness and Safety of Bioresorbable Vascular Scaffold in Routine Clinical Practice; A Multicenter, Prospective Observational Study
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 629 (actual)
- Sponsor
- Duk-Woo Park, MD · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the relative effectiveness and safety of Bioresorbable Vascular Scaffold compared to other (drug eluting stents) DES.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Bioresorbable Vascular Scaffold |
Timeline
- Start date
- 2016-02-26
- Primary completion
- 2019-03-23
- Completion
- 2023-12-01
- First posted
- 2015-12-04
- Last updated
- 2023-12-20
Locations
14 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02622100. Inclusion in this directory is not an endorsement.