Biotronik

NCT01531725

MULTIcentric BElgium/NEtherlands PRO-Kinetic Safety and Efficacy Study

NCT01459874

Evaluation of an Organizational Model for Remote Monitoring of Pacemaker and Implantable Cardioverter Defibrillator Recipients

NCT00961181

Paclitaxel Releasing Balloon in Patients Presenting With In-Stent Restenosis

NCT01056120

Long Term Safety Profile of the PRO-Kinetic ENERGY Coronary Stent System in Daily Clinical Practice

NCT01081366

Drug Eluting Pantera Lux Catheter Registry

NCT01168830

First in Man Trial - BIOSOLVE-I

NCT01221610

BIOLUX P-I First in Man Study

NCT01356888

Study of the Orsiro Drug Eluting Stent System

NCT01610102

PROGRESS-AMS 1.0 Clinical Long Term Follow-Up

NCT01426139

BIOFLOW-INDIA Safety and Clinical PerFormance of the Drug Eluting ORSIRO Stent in Single de Novo Coronary Artery Lesions

NCT01553526

BIOFLOW-III All-comers Orsiro Safety and Performance Registry

NCT01443104

Sirolimus-eluting Stents With Biodegradable Polymer Versus an Everolimus-eluting Stents

NCT01651390

Clinical Performance of the Pantera Lux Balloon Versus the Orsiro Stent in Patients With In-stent Restenosis.

NCT01867736

BIOLUX P-II First-in-Man Study to Compare the Passeo-18 Lux DRB Against POBA in Infrapopliteal Arteries

NCT01667003

BIOFLOW-III Sweden Satellite Registry

NCT01661231

Study to Determine the Performance of the Astron and Pulsar-18 Stents in Europe

NCT01811927

The Treatment of Coronary Artery Lesions Using the PRO-Kinetic Energy Cobalt-Chromium, Bare-Metal Stent

NCT01939249

Prospective, Randomized, Multicenter Study to Assess the Safety and Effectiveness of the Orsiro Sirolimus-eluting Stent

NCT01960504

First in Man Study of the DREAMS 2nd Generation Drug Eluting Absorbable Metal Scaffold (BIOSOLVE-II)

NCT02249000

BIOVALVE - I / II Clincial Investigation

NCT02276313

BIOLUX P-III All-Comers Passeo-18 Lux Registry

NCT02389946

Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions

NCT02716220

Pre-market Study of the DREAMS 2G Drug Eluting Absorbable Metal Scaffold (BIOSOLVE-III)

NCT02817802

BIOTRONIKS - Safety and Performance in de NOvo Lesion of NatiVE Coronary Arteries With Magmaris- Registry: BIOSOLVE-IV

NCT03052309

BIOLUX P-III BENELUX All-Comers Registry

NCT03044002

BIOTRONIK 4French for AMBulatory Peripheral Intervention

NCT03052296

BIOLUX P-III SPAIN All-Comers Registry

NCT02247492

BIOFLOW-III VIP Russia Registry Orsiro Stent System

NCT02916485

Safety and Clinical Performance of a Sirolimus-eluting Absorbable Metal Scaffold

NCT03263858

Vascular Implant Safety and Efficacy Study

NCT03298659

iFR Guided Multi-vessel Revascularization During Percutaneous Coronary Intervention for Acute Myocardial Infarction

NCT03600961

BIOFLOW-SV Portugal Registry

NCT03600948

BIOFLOW-SV All Comers Registry

NCT03547986

BIO REsponse Adapted Combination Therapy Pilot Study

NCT04250909

Retrospective Follow-up of BIOLUX P-I/-II

NCT04157153

First in Men Study: BIOMAG-I

NCT04555174

BIOFLOW-VIII All-comers Orsiro Mission Safety and Performance Registry

NCT04679740

Resorbable Magnesium Scaffolds Registry

NCT04525794

BRight DCB First-in-Human Study

NCT04830228

BIOTRONIK Dynetic-35 Stent for the Treatment of Peripheral Iliac Lesions

NCT05831319

Evaluation of Standard of Care Practices, Procedural Outcomes and In-hospital Complications of Peripheral Endovascular Procedures

NCT05667285

BIOFLOW-china Post-marketing Study (BIOTRONIK)

NCT05540223

Safety and Clinical Performance of the DREAMS 3G Resorbable Magnesium Scaffold System

NCT06758921

Prospective, Multicenter, Single-Arm Observational Study to Confirm the Safety and Clinical Performance of the Oscar Peripheral Multifunctional Catheter for the Dilatation of Lesions in the Femoral, Popliteal and Infrapopliteal Arteries (BIO-OSCAR First)

NCT07091682

Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System in the Treatment of Subjects With Long de Novo Lesions

NCT06779630

Safety and Effectiveness of the Orsiro Mission 48-mm Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions (BIOFLOW-48) Study