Clinical comparison study between newly developed FFR device based on optical interferometry and conventional FFR device
Not Applicable
- Conditions
- coronary artery disease patients
- Registration Number
- JPRN-UMIN000028268
- Lead Sponsor
- Department of Cardiology Aichi Medical University
- Brief Summary
https://www.ncbi.nlm.nih.gov/pubmed/31913164
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 51
Inclusion Criteria
Not provided
Exclusion Criteria
1. AV block 2. bronchial asthma
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Evaluation of Safety use of newly FFR devise 2. Evaluation of Fractional Flow Reserve
- Secondary Outcome Measures
Name Time Method