Trials / Completed
CompletedNCT01348399
Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME)
Evaluation of Effectiveness and Safety of XIENCE PRIME™ in Routine Clinical Practice; A Multicenter, Prospective Observational Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 2,000 (actual)
- Sponsor
- Seung-Jung Park · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate effectiveness and safety of XIENCE PRIME stent in the "real world" daily practice as compared with other drug eluting stents (DESs)
Detailed description
This study is a non-randomized, prospective, open-label registry to compare the effectiveness and safety of XIENCE PRIME stents versus other DESs in patients with coronary artery disease.
Conditions
Timeline
- Start date
- 2011-04-01
- Primary completion
- 2014-07-01
- Completion
- 2017-09-01
- First posted
- 2011-05-05
- Last updated
- 2018-06-20
Locations
29 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01348399. Inclusion in this directory is not an endorsement.