IRIS-Onyx Cohort in the IRIS-DES Registry

RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort)

NCT03584464 ·Status: COMPLETED ·Phase: NA

A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk Patients Who Are Considered One-Month Clear (Onyx ONE Clear)

NCT03647475 ·Status: COMPLETED ·Phase: NA

IRIS-Firehawk® Cohort in the IRIS-DES Registry

NCT03380286 ·Status: WITHDRAWN

Biofreedom Prospective Multicenter Observational Registry

NCT03045848 ·Status: TERMINATED

Prospective, Multi-center, Single-arm Study of the Auryon Laser System for Treatment of Below-the-Knee (BTK) Arteries

NCT05284240 ·Status: COMPLETED ·Phase: NA

REWARDS Premier Taxus-Liberte vs Xience V

NCT02256527 ·Status: COMPLETED

Korean Multicenter Registry of EPIC Stent for Iliac Artery Disease: (K-EPIC Registry)

NCT02698358 ·Status: UNKNOWN

A Prospective Single-Arm Multicenter StuDy of the BarE TEmporary SPur StEnt System foR the tREatment of Vascular Lesions Located in the infrapoplitEal Arteries beLow the Knee (DEEPER REVEAL)

NCT05358353 ·Status: COMPLETED ·Phase: NA

Evaluation of the Safety and Effectiveness of the CorPath 200 System in Percutaneous Coronary Interventions (PCI)

NCT01275092 ·Status: COMPLETED ·Phase: PHASE2

The Complete® Self-Expanding Stent and Stent Delivery System Registry

NCT00730730 ·Status: COMPLETED ·Phase: NA

Efficacy and Safety of 1-year Duration of DAPT After GENOSS® DES Implantation in Patients with Coronary Artery Disease According to the Complex Higher-risk Procedure

NCT06075433 ·Status: RECRUITING

To Evaluate Safety and Efficacy of CGBIO Stent Compared to Biomatrix Flex Stent

NCT03089450 ·Status: UNKNOWN ·Phase: NA

RevCore for In Stent Thrombosis

NCT06394739 ·Status: RECRUITING

Randomised Trial of Dual Device Treatment Involving Drug-coated Balloon Angioplasty and Drug-eluting Stent Implantation Compared to Single Device Treatments in Patients With Diabetes Mellitus

NCT07303439 ·Status: RECRUITING ·Phase: NA

ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2

NCT05072730 ·Status: RECRUITING ·Phase: NA

Assessment of GORE® EXCLUDER® IBE Plus Stent Graft Performance in Patients Undergoing Endovascular Iliac Revascularization

NCT07304102 ·Status: NOT_YET_RECRUITING ·Phase: NA

Initial Feasibility Study of the STENTiT Resorbable Fibrillated Scaffold (RFS). The RFS is Intended to Restore Lumen Patency and Blood Flow to Infrapopliteal Arteries. The RFS is a Fully Electrospun Tubular Device With a Fibrillated Microarchitecture and Designed for Transcatheter Delivery

NCT07006467 ·Status: RECRUITING ·Phase: NA

Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With Coronary Artery Lesions

NCT07258290 ·Status: NOT_YET_RECRUITING ·Phase: NA

Safety and Effectiveness of the Peripheral Balloon-Expandable Covered Stent System for Iliac Artery Stenosis/Occlusion. (SELECT)

NCT06605209 ·Status: RECRUITING ·Phase: NA

Safety and Effectiveness of Surgeon-Modified Stent Grafts forTreatment of Complex Aortic Aneurysms

NCT05531084 ·Status: NOT_YET_RECRUITING ·Phase: NA

DCS Versus DES for One-month DAPT in Patients With ACS: ONE-PASS Trial

NCT05305482 ·Status: RECRUITING ·Phase: NA

An International Registry of the Wingspan™ Stent System for the Treatment of Intracranial Atherosclerotic Stenosis

NCT00929383 ·Status: COMPLETED

Safety and Effectiveness of GENOSS® DES in Patients With Multivessel Coronary Artery Disease

NCT06168305 ·Status: ENROLLING_BY_INVITATION

Safety and Efficacy of IrisFIT™ Patent Foramen Ovale Occluders

NCT05312554 ·Status: WITHDRAWN ·Phase: NA

An Observational Registry Using Drug Eluting Stents (DES) in Patients in a Real-World Setting (DEScover Registry).

NCT00489320 ·Status: COMPLETED