Biotronik SE & Co. KG: all 187 studies
Page 2 of 2. Open to participants first (9), then studies with results posted, then the rest; newest registration first within each.
- BIOTRONIKS - Safety and Performance in de NOvo Lesion of NatiVE Coronary Arteries With Magmaris- Registry: BIOSOLVE-IVActive, not recruitingNCT02817802
- Pre-market Study of the DREAMS 2G Drug Eluting Absorbable Metal Scaffold (BIOSOLVE-III)CompletedNCT02716220Not applicable
- Clinical Benefits of the Closed Loop Stimulation in Sinus Node DiseaseTerminatedNCT02579889Not applicable
- BIO.MASTER.BioMonitor 2 StudyCompletedNCT02565238
- ProMRI 3T ENHANCED Master StudyCompletedNCT02506569
- Preventive aBlation of vEntricular tachycaRdia in Patients With myocardiaL INfarctionTerminatedNCT02501005Not applicable
- Registry Study of Clinical Application of MRI Compatible CIEDCompletedNCT02380300
- Clinical Investigation on Differences in the Magnitude of CRT Response in WOmen Versus MENCompletedNCT02344420Not applicable
- Assessment of Ventricular Arrhythmia Risk After CRT-D Replacement for Patients With Primary Prevention IndicationCompletedNCT02323503
- BIOLUX P-III All-Comers Passeo-18 Lux RegistryCompletedNCT02276313
- Reduction of AF Ablation Induced Thrombo-Embolic Incidence Pilot StudyTerminatedNCT02275260Not applicable
- BIOTRONIK - BIOFLOW-III Registry French SatelliteStatus unknownNCT02273648
- BIOFLOW-III UK Satellite Registry Orsiro Stent SystemStatus unknownNCT02257710
- BIOVALVE - I / II Clincial InvestigationCompletedNCT02249000Not applicable
- BIOFLOW-III VIP Russia Registry Orsiro Stent SystemStatus unknownNCT02247492
- Iperia/Sentus QP StudyCompletedNCT02181686
- Assessment of Intracardiac Electrograms Transmitted by Home Monitoring for the Remote Follow-up of Pacemaker (PREMS)CompletedNCT02174484
- Eluna Family / Sentus BP Master StudyCompletedNCT02059629
- BIOFLOW III Satellite-ELADIS Orsiro Stent SystemCompletedNCT02029092
- BIOFLOW III Satellite-Italy Orsiro Stent SystemCompletedNCT02028728
- SD01 Registry (SD01 ICD Lead)CompletedNCT02014675
- First in Man Study of the DREAMS 2nd Generation Drug Eluting Absorbable Metal Scaffold (BIOSOLVE-II)Status unknownNCT01960504Not applicable
- BIOFLOW III Asia Registry Orsiro Stent SystemCompletedNCT01941290
- Prospective, Randomized, Multicenter Study to Assess the Safety and Effectiveness of the Orsiro Sirolimus-eluting StentStatus unknownNCT01939249Not applicable
- PaneLux PTCA : Proposing an Alternative Treatment to patiEnts for Whom DES Implantation is Not Indicated, Thanks to Pantera LUX Drug Eluting BalloonStatus unknownNCT01930903Not applicable
- Post Market Clinical Follow-up of CRT-DX Therapy With Lumax 640/740 HF-TCompletedNCT01930695
- BIOFLOW-III Israel Satellite RegistryCompletedNCT01895712
- BIOFLOW-III Hungary Satellite RegistryTerminatedNCT01892917
- BIOFLOW-III Canada Satellite RegistryCompletedNCT01880242
- BIOLUX P-II First-in-Man Study to Compare the Passeo-18 Lux DRB Against POBA in Infrapopliteal ArteriesCompletedNCT01867736Not applicable
- Selection of Potential Predictors of Worsening Heart FailureCompletedNCT01836510
- SD01 Master Study (Safety and Efficacy Study)CompletedNCT01836497
- BIOFLOW-III Belgium Satellite RegistryCompletedNCT01831336
- The Treatment of Coronary Artery Lesions Using the PRO-Kinetic Energy Cobalt-Chromium, Bare-Metal StentTerminatedNCT01811927Not applicable
- ProMRI PROVEN Master StudyCompletedNCT01809665
- DF4 Master Study (Safety and Efficacy Study)CompletedNCT01790841
- Management and Detection of Atrial Tachyarrhythmias in Patients Implanted With BIOTRONIK DX SystemsCompletedNCT01774357
- BioMonitor Master StudyCompletedNCT01725568
- Monitoring of Hemodynamics in Heart Failure Patients by Intracardiac Impedance MeasurementCompletedNCT01711281Phase 4
- BIOFLOW-III Austria Satellite RegistryCompletedNCT01667016
- BIOFLOW-III Sweden Satellite RegistryCompletedNCT01667003
- Study to Determine the Performance of the Astron and Pulsar-18 Stents in EuropeStatus unknownNCT01661231Not applicable
- Clinical Performance of the Pantera Lux Balloon Versus the Orsiro Stent in Patients With In-stent Restenosis.CompletedNCT01651390Not applicable
- PROGRESS-AMS 1.0 Clinical Long Term Follow-UpCompletedNCT01610102
- Ability of Home Monitoring® to Detect and Manage the Inappropriate Diagnoses in Implantable Cardioverter Defibrillators.CompletedNCT01594112
- BIOFLOW-III Romania Satellite RegistryTerminatedNCT01593059
- BIOFLOW-III All-comers Orsiro Safety and Performance RegistryStatus unknownNCT01553526
- Evia/Entovis HF-T Master StudyCompletedNCT01545739
- Ventricular Pace Suppression Versus Intrinsic Rhythm Support StudyCompletedNCT01528657Not applicable
- Setrox JS Master StudyCompletedNCT01487941
- Lumax DX / Linox DX EvaluationCompletedNCT01486836
- ProMRI AFFIRM Study of the EVIA/ENTOVIS Pacemaker With Safio S Pacemaker LeadsCompletedNCT01460992
- Lumax 740 Master StudyCompletedNCT01454050
- BIOFLOW-INDIA Safety and Clinical PerFormance of the Drug Eluting ORSIRO Stent in Single de Novo Coronary Artery LesionsCompletedNCT01426139Not applicable
- Clinical Registry on Sudden Death Primary Prevention at Latin AmericaWithdrawnNCT01422174
- Study of the Orsiro Drug Eluting Stent SystemStatus unknownNCT01356888Not applicable
- NORDIC ICD (Cardioverter Defibrillator Implantation) TrialCompletedNCT01282918Not applicable
- Monitoring of Fluid Status in Heart Failure Patients by Intrathoracic Impedance Measurement in Japan (J-HomeCARE II)CompletedNCT01221649Phase 4
- BIOLUX P-I First in Man StudyCompletedNCT01221610Not applicable
- First in Man Experience With a Drug Eluting Stent in De Novo Coronary Artery LesionsCompletedNCT01214148Phase 1/2
- First in Man Trial - BIOSOLVE-ICompletedNCT01168830Not applicable
- Genotyping Infarct Patients to Adjust and Normalize Thienopyridine TreatmentCompletedNCT01134380
- Strategy of Early Detection and Active Management of Supraventricular Arrhythmia With Telecardiology (SETAM)CompletedNCT01108692Not applicable
- Linox Smart S DX PME/Master StudyCompletedNCT01090401Phase 4
- Drug Eluting Pantera Lux Catheter RegistryCompletedNCT01081366
- Long Term Safety Profile of the PRO-Kinetic ENERGY Coronary Stent System in Daily Clinical PracticeCompletedNCT01056120
- Ventricular Pace Suppression StudyCompletedNCT01053832Not applicable
- Observational Study of Patient Comprehension, Perception, Fears and Appreciation Following Home-Monitoring ImplementationCompletedNCT01006746
- SIELLO Pilot Study for Comparison of Steroid Versus Non-Steroid Pacing LeadsCompletedNCT01000532
- Benefits of Implantable Cardioverter Defibrillator Follow-up Using Remote MonitoringCompletedNCT00989417Not applicable
- Evaluate the Benefits of Pacemaker Follow-Up With Home-MonitoringCompletedNCT00989326Not applicable
- Master Study for the Investigation of Safety and Efficacy of the SIELLO Pacemaker LeadsCompletedNCT00943046Not applicable
- Self Expanding Nitinol Stent Versus Percutaneous Transluminal Arterial Angioplasty (PTA) With Optional Bailout Stenting in Case of PTA Failure in Patients With Symptomatic Critical Limb Ischemia or Severe Intermittent Claudication (EXPAND)CompletedNCT00906022Phase 4
- Follow-up of Patients With Implantable Cardioverter Defibrillators by Home Monitoring (ANVITE)TerminatedNCT00858559Not applicable
- European Health Economic Trial on Home Monitoring in ICD and CRT-D Patients (EuroEco)TerminatedNCT00776087Not applicable
- Monitoring of Fluid Status in Heart Failure Patients by Intrathoracic Impedance Measurement (HomeCARE II)CompletedNCT00711360Phase 4
- Catheter Ablation vs. Standard Conventional Treatment in Patients With LV Dysfunction and AFCompletedNCT00643188Phase 4
- Comparison of Best Medical Treatment Versus Best Medical Treatment Plus Renal Artery StentingCompletedNCT00640406Phase 3
- Survival of Patients With Primary Prophylactic ICD IndicationCompletedNCT00619593Phase 4
- Fast VT Episodes Are Terminated by ATP One ShotCompletedNCT00617578Phase 4
- Influence of Home Monitoring on the Clinical Status of Heart Failure Patients With an Impaired Left Ventricular FunctionCompletedNCT00538356Phase 4
- Virtual Clinic Pacemaker Follow-upTerminatedNCT00475124Phase 4
- Remote Follow-up of Patients Receiving Implantable Cardioverter Defibrillator for Prophylactic TherapyCompletedNCT00401466Phase 4
- Home Monitoring in Cardiac Resynchronisation TherapyCompletedNCT00376116
- Psychosomatic Effects of Implantable Cardioverter Defibrillator With Home Monitoring Function (QUANTUM)CompletedNCT00325221Not applicable
- Study to Verify Proper Detection of Supraventricular Tachyarrhythmia With Single-Lead Dual-Chamber Implantable Cardioverter-Defibrillators (ADRIA)CompletedNCT00324662Phase 4
- Closed Loop Stimulation, Cognitive Performance, and Quality of Life in Pacemaker PatientsCompletedNCT00323661Phase 4