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A Post-Approval, Single-Arm Study of the SYNERGY Stent System in China
Sponsor: Boston Scientific Corporation
Summary
A prospective, observational, single-arm, open-label, multicenter, post-approval study. To compile real-world clinical outcomes data for the SYNERGYTM MONORAILTM Everolimus-Eluting Platinum Chromium Coronary Stent System (SYNERGYTM Stent System) in real-world clinical practice in China.
Official title: A Post-Approval, Single-Arm Study of the SYNERGYTM MONORAILTM Everolimus-Eluting Platinum Chromium Coronary Stent System in China
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
2000
Start Date
2019-07-30
Completion Date
2028-03-31
Last Updated
2026-03-24
Healthy Volunteers
No
Conditions
Interventions
SYNERGYTM Stent System
no intervention design in the study
Locations (1)
Zhongshan Hospital Fudan University
Shanghai, Shanghai Municipality, China