A Post-Approval, Single-Arm Study of the SYNERGY Stent System in China
Active, not recruiting
- Conditions
- Cardiovascular Diseases
- Registration Number
- NCT03736226
- Lead Sponsor
- Boston Scientific Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Active, not recruiting
- Sex
- All
- Target Recruitment
- 2000
Inclusion Criteria
Inclusion Criteria:<br><br> - • Subject must be at least 18 years of age<br><br> - Subject understands and provides written informed consent<br><br> - Subject who is clinically indicated and will have an attempt of at least one<br> SYNERGYTM stent OR Subject who is clinically indicated and was implanted with<br> at least one SYNERGYTM stent<br><br> - Subject is willing to comply with all protocol-required follow-up evaluation<br><br>Exclusion Criteria:<br><br> - Exclusion criteria are not required in this study which is an all comers study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Observational [Patient Registry]
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method MACE rate
- Secondary Outcome Measures
Name Time Method