DESyne in Routine Clinical Practice
NCT02039713 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 342
Last updated 2021-09-13
Summary
The purpose of this study is to evaluate effectiveness and safety of DESyne in Routine Clinical Practice
Conditions
- Angioplasty, Transluminal, Percutaneous Coronary
- Coronary Artery Disease
Interventions
- DEVICE
-
DeSyne drug eluting stent group
Sponsors & Collaborators
-
CardioVascular Research Foundation, Korea
collaborator OTHER -
Amg Korea Co. Ltd.
collaborator INDUSTRY -
Seung-Jung Park
lead OTHER
Eligibility
- Min Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-07-31
- Primary Completion
- 2018-03-31
- Completion
- 2018-03-31
Countries
- South Korea
Study Locations
More Related Trials
-
Evaluation of Effectiveness and Safety of XIENCE Sierra in Routine Clinical Practice
NCT03967158 ·Status: ACTIVE_NOT_RECRUITING
-
Assessment of Dual AntiPlatelet Therapy With Drug Eluting Stents
NCT00638794 ·Status: COMPLETED
-
Prospective Assessment of Efficacy and Safety of Drug Eluting Stents
NCT02313038 ·Status: COMPLETED
-
Safety and Efficacy of Paclitax Coated Balloon in Patients With Coronary In-stent Restenosis (ISR)
NCT05656118 ·Status: ACTIVE_NOT_RECRUITING
-
The DESyne BDS Plus RCT: A Randomized Clinical Trial to Assess the Elixir DESyne BDS Plus Drug Eluting Coronary Stent System for the Treatment of de Novo Native Coronary Artery Lesions
NCT05033964 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Orsiro™ Drug Eluting Stent in Routine Clinical Practice
NCT02039739 ·Status: COMPLETED
-
IRIS-Synergy Cohort in the IRIS-DES Registry
NCT02720419 ·Status: ACTIVE_NOT_RECRUITING
-
Drug-Coated Balloon in Combination With New Generation Drug-Eluting Stent for de Novo Diffuse Disease Treatment
NCT03939468 ·Status: UNKNOWN
-
Genoss DES in Patients With a High Risk of Ischemic Events (GENTLE Registry)
NCT05448625 ·Status: COMPLETED
-
Outcome of Second Generation Drug-eLuting Stents in Patients With Diabetes Mellitus
NCT01293773 ·Status: WITHDRAWN ·Phase: PHASE4
-
DEB Versus 2nd Generation DES in Patients With In-Scaffold Restenosis of Bioresorbable Vascular Scaffold
NCT03074305 ·Status: WITHDRAWN ·Phase: NA
-
Drug Eluting Balloon Efficacy for Small Coronary Vessel Disease Treatment
NCT03899818 ·Status: COMPLETED ·Phase: NA
-
The Clinical Efficacy and Safety of Drug-coated Balloon
NCT05133921 ·Status: COMPLETED
-
Genoss DES Prospective Multicenter Registry
NCT03045913 ·Status: COMPLETED
-
Comparison of Safety and Efficacy of Coronary Drug-coated Balloon (DCB) Combined With Spot Stenting of Drug-eluting Stent (DES) Versus Second-generation DES for Treating Diffuse Coronary Artery Lesions: a Prospective, Randomized, Controlled Clinical Trial
NCT03589157 ·Status: UNKNOWN ·Phase: NA
-
International Randomized Comparison Between DES Limus Carbostent and Taxus DES in the Treatment of De-novo Coronary Lesions
NCT01373502 ·Status: COMPLETED ·Phase: NA
-
Safety and Performance Assessment of Drug-Eluting Stent CRE8 in Diabetic Patients
NCT03842813 ·Status: UNKNOWN
-
A Safety and Efficacy Study of Dissolve™ in Treatment of Coronary Small Vessel Disease
NCT03376646 ·Status: COMPLETED ·Phase: NA
-
Joint Inflation With Nominal-pressure and Stability Approach in DES Optimization
NCT06013007 ·Status: COMPLETED ·Phase: NA
-
Dexamethasone-Eluting Stent in Acute Coronary Syndrome to Prevent Restenosis
NCT00190099 ·Status: COMPLETED ·Phase: PHASE4
-
Diffuse Type In-Stent Restenosis After Drug-Eluting Stent
NCT00485030 ·Status: COMPLETED ·Phase: PHASE4
-
Comparison of a Contemporary Sirolimus-eluting Stent (ihtDEStiny®) With Another Everolimus-eluting Stent (Xience™), Both With Permanent Polymers, in Patients With Acute Coronary Syndrome and de Novo Coronary Artery Lesions
NCT07190690 ·Status: RECRUITING ·Phase: NA
-
Intimal Hyperplasia Evaluated by Optical Coherence Tomography (OCT) in de Novo Coronary Lesions Treated by Drug-eluting Balloon and Bare-metal Stent
NCT01057563 ·Status: UNKNOWN ·Phase: PHASE4
-
Drug-Eluting Stent Implantation Versus Optimal Medical Treatment in Patients With Chronic Total Occlusion (DECISION-CTO)
NCT01078051 ·Status: TERMINATED ·Phase: PHASE4
-
Vascular Healing of DES at 3 Months
NCT01391871 ·Status: COMPLETED