Biotronik SE & Co. KG: all 187 studies

Page 1 of 2. Open to participants first (9), then studies with results posted, then the rest; newest registration first within each.

• BIO|STREAM.CSP CLSRecruitingNCT07608822
• BIO|STREAM.CSP StudyRecruitingNCT07393009
• BIO|MASTER.CorSky Family Post-market Study for the CorSky Family of ICDsRecruitingNCT07360158
• BIOTRONIK Investigation of the LivIQ Leadless Pacemaker SystemRecruitingNCT07118358Not applicable
• BIO|CONCEPT.BIOMONITOR-HF Collect Clinical Data From Heart Failure Patients Using BIOMONITOR Devices With a Study Specific Research SoftwareRecruitingNCT06989580Not applicable
• 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)RecruitingNCT06758921
• Post-market Clinical Follow-up Data Collection From Procedures With BIOTRONIK EP ProductsRecruitingNCT05560958
• Resorbable Magnesium Scaffolds RegistryRecruitingNCT04679740
• Observation of Clinical Routine Care for Patients With BIOTRONIK Implantable Cardiac Monitors (ICMs)RecruitingNCT04075084
• Head-up Tilt Test in Patients With Reflex Syncope and Asystolic Response Who Received a Dual-chamber Pacemaker With the Closed Loop Stimulation (CLS) and Participated in the BIOSync TrialCompletedNCT06038708Results posted
• BIOSTREAM.HF HeartInsightCompletedNCT05761249Results posted
• BIO|CONCEPT.Amvia StudyCompletedNCT05610176Not applicableResults posted
• BIOTRONIK Conduction System Pacing With the Solia LeadCompletedNCT05251363Not applicableResults posted
• Full Early Atrial Diagnostics in Single Chamber ICD Patients Using the DX Lead and Home Monitoring in Brazil.CompletedNCT04869527Results posted
• Qubic Stim Cardiac Stimulator in ChinaCompletedNCT04390841Not applicableResults posted
• BIO|CONCEPT.Renamic Neo StudyCompletedNCT04350008Results posted
• BIO|CONCEPT.ECG-Library (Collection of ECG Signals for Development of Algorithms)TerminatedNCT04243070Not applicableResults posted
• Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery LesionsCompletedNCT04175626Results posted
• Assessment of the Utility of BIOMONITOR to Identify Atrial Fibrillation (AF) in Ablation Candidates Using Precise AF DetectionTerminatedNCT04076917Results posted
• Master Study of the BIOMONITOR III and Incision and Insertion Tool (FIT OneStep)CompletedNCT04025710Not applicableResults posted
• Master Study of the Acticor/Rivacor ICDs/CRT-Ds and the Plexa ProMRI S DX LeadCompletedNCT03891329Not applicableResults posted
• Comparison of the Effects of Two Spinal Cord Stimulation (SCS) Therapies on Subject Reported Pain (BENEFIT-02)CompletedNCT03594266Not applicableResults posted
• QP ExCELs: MultiPole Pacing (MPP) Sub-StudyCompletedNCT03155724Not applicableResults posted
• Plexa ICD Lead RegistryTerminatedNCT03103503Results posted
• BIOTRONIK Orsiro Pre-Marketing RegistrationCompletedNCT02870985Not applicableResults posted
• BIO|MASTER.Ilivia Family / PlexaCompletedNCT02774616Not applicableResults posted
• BioMonitor 2 In-Office Setting Insertion Safety and Feasibility Evaluation With Device Functionality AssessmentCompletedNCT02756338Results posted
• Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery LesionsCompletedNCT02389946Not applicableResults posted
• BIO monitorinG in Patients With Preserved Left ventricUlar Function AfteR Diagnosed Myocardial InfarctionCompletedNCT02341534Not applicableResults posted
• Benefit of Dual-chamber Pacing With Closed Loop Stimulation (CLS) in Tilt-induced Cardioinhibitory Reflex SyncopeCompletedNCT02324920Not applicableResults posted
• Sentus QP - Extended CRT Evaluation With Quadripolar Left Ventricular LeadsTerminatedNCT02290028Not applicableResults posted
• Protego DF4 Post Approval RegistryTerminatedNCT02243696Results posted
• ProMRI Study of the Iforia ICD System (Phase C)CompletedNCT02096692Results posted
• TD01 Master Study (Safety and Efficacy Study)CompletedNCT02087189Results posted
• ProMRI Study of the Entovis Pacemaker System (Phase B)CompletedNCT02009696Results posted
• Safety and Performance Study of the Siello S Pacing LeadTerminatedNCT01791127Results posted
• ProMRI Study of the Entovis Pacemaker SystemCompletedNCT01761162Results posted
• BIOHELIX-I Bare Metal Stent StudyCompletedNCT01612767Phase 2/3Results posted
• MULTIcentric BElgium/NEtherlands PRO-Kinetic Safety and Efficacy StudyCompletedNCT01531725Not applicableResults posted
• Safety and Efficacy Study of IPG Patient With Home MonitoringCompletedNCT01523704Not applicableResults posted
• Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar StentsCompletedNCT01319812Phase 2Results posted
• Paclitaxel Releasing Balloon in Patients Presenting With In-Stent RestenosisCompletedNCT00961181Not applicableResults posted
• Master Study for the Investigation of Safety and Efficacy of the EVIA PacemakerCompletedNCT00916344Not applicableResults posted
• Long-term Evaluation of the Linox Family ICD Leads Registry (GALAXY)CompletedNCT00836589Results posted
• Clinical effecT of Heart Failure Management Via Home Monitoring With a Focus on Atrial Fibrillation (effecT)TerminatedNCT00811382Not applicableResults posted
• Post Approval Registry of Corox OTW, Endocardial, Left Ventricular Steroid Lead, BipolarCompletedNCT00810264Results posted
• Echocardiography Guided Cardiac Resynchronization Therapy (EchoCRT)TerminatedNCT00683696Phase 2/3Results posted
• Combined Use of BIOTRONIK Home Monitoring and Predefined Anticoagulation to Reduce Stroke RiskTerminatedNCT00559988Phase 4Results posted
• Interventricular Delay of Lumax HF-T for Heart FailureCompletedNCT00508391Phase 2Results posted
• COSMO Post Approval Registry: Corox OTW Steroid LV Lead MonitoringCompletedNCT00396136Phase 4Results posted
• TRIAGE-CRT Telemonitoring in Patients With CHF and Indication of CRT-DCompletedNCT00395642Phase 4Results posted
• REPLACE: Implantable Cardiac Pulse Generator Replacement RegistryCompletedNCT00395447Results posted
• Investigational Device Exemption (IDE) Study for the Approval of Closed Loop Stimulation (CLS) and Cardiac Resyncronization Pacing Therapies (CRT) for the Treatment of Atrial Fibrillation (AF) With Ablate and PaceTerminatedNCT00356057Not applicableResults posted
• Effectiveness of Pacemaker With Closed Loop Stimulation Compared to Pacemakers With and Without Standard Rate ResponseCompletedNCT00355797Phase 4Results posted
• TRUST: Lumos-T Safely RedUceS RouTine Office Device Follow-upCompletedNCT00336284Phase 4Results posted
• Isthmus Ablation With Gold Electrode for Treatment of Atrial Flutter (AURUM 8)CompletedNCT00326001Phase 4Results posted
• Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System in the Treatment of Subjects With Long de Novo LesionsActive, not recruitingNCT07091682Not applicable
• BIO|CONCEPT.CorSky, First in Human Study for the CorSky ICD FamilyActive, not recruitingNCT06840509Not applicable
• BIO|MASTER.CSP StudyActive, not recruitingNCT06620237Not applicable
• BIOTRONIK Conduction System Pacing With the Solia Lead - Solia CSP SCompletedNCT06540079Not applicable
• BRight Pharmacokinetic StudyCompletedNCT06065345Not applicable
• Post Market Clinical Follow-up Study for the Amvia/Solvia Pacemaker FamilyCompletedNCT06018818Not applicable
• Evaluation of Standard of Care Practices, Procedural Outcomes and In-hospital Complications of Peripheral Endovascular ProceduresCompletedNCT05831319
• BIOFLOW-china Post-marketing Study (BIOTRONIK)TerminatedNCT05667285
• Post Market Clinical Follow-up Study for the Pamira ICD Lead FamilyCompletedNCT05621187Not applicable
• Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold SystemActive, not recruitingNCT05540223Not applicable
• To Evaluate the Delivery Timing Safety and Efficacy of AntiTachycardia Pacing (BIO|ATP)Active, not recruitingNCT05426785Not applicable
• One Day Implantation Program for Heart Failure Patients Implanted With CRT-PCompletedNCT05142293
• Atrial Fibrillation Associated With Heart Failure Treated by BIOTRONIK's CRT-DX SystemTerminatedNCT04870281
• BIOTRONIK Dynetic-35 Stent for the Treatment of Peripheral Iliac LesionsActive, not recruitingNCT04830228
• Evaluation of the BIOTRONIK AutoAdapt Algorithm for Continuous Automatic Adaptive Cardiac ResynchronizationCompletedNCT04774523Not applicable
• A First in Human Feasibility Study to Evaluate the Safety and Effectiveness of the BIOTRONIK Prospera SCS System with HomeStream Remote ManagementActive, not recruitingNCT04683718Not applicable
• BIOFLOW-VIII All-comers Orsiro Mission Safety and Performance RegistryActive, not recruitingNCT04555174
• BRight DCB First-in-Human StudyCompletedNCT04525794Not applicable
• Master Study Investigating the Guiding Catheter Selectra 3DCompletedNCT04323670Not applicable
• Retrospective Follow-up of BIOLUX P-I/-IICompletedNCT04250909
• BIO|STREAM.ICM FranceCompletedNCT04206774
• BIO|STREAM.ICM ObesityCompletedNCT04198220
• First in Men Study: BIOMAG-IActive, not recruitingNCT04157153Not applicable
• Bioflow-DAPT StudyCompletedNCT04137510Phase 4
• Assessment of Risk Factors for Appropriate ICD (Implantable Cardioverter-defibrillator) Intervention in Patients With Ischemic CardiomyopathyCompletedNCT04014946Not applicable
• Analysis of Both Sex and Device Specific Factors on Outcomes in Patients with Non-Ischemic CardiomyopathyCompletedNCT03884608
• BIO|CONCEPT.BIOMONITOR IIICompletedNCT03850327Not applicable
• Safety and Performance Aspects of CRT-DX System in Patients With Sinus RhythmCompletedNCT03839121
• BIOFLOW-SV Portugal RegistryTerminatedNCT03600961
• BIOFLOW-SV All Comers RegistryTerminatedNCT03600948
• BIO REsponse Adapted Combination Therapy Pilot StudyStatus unknownNCT03547986Not applicable
• Observation of Clinical Routine Care for Heart Failure Patients Implanted With BIOTRONIK CRT DevicesActive, not recruitingNCT03366545
• A Prospective Pilot Study (BIO|SELECT Pilot)CompletedNCT03337763
• Assessment of Pacing Stimulus Conduction and Latency Measurements in CRT-D PatientsTerminatedNCT03314675Not applicable
• Vascular Implant Safety and Efficacy StudyCompletedNCT03263858Not applicable
• Pilot Study to Investigate the Creation of Physiological Rhythm by Closed Loop Stimulation in hEart Failure pAtients With chronoTropic incompEtenceCompletedNCT03157076Not applicable
• BIO|MASTER.Edora Family StudyCompletedNCT03091322
• BIOLUX P-III BENELUX All-Comers RegistryCompletedNCT03052309
• BIOLUX P-III SPAIN All-Comers RegistryCompletedNCT03052296
• Clinical Investigation Plan for the AVOPT Data Collection Clinical StudyCompletedNCT03049722Not applicable
• BIOTRONIK 4French for AMBulatory Peripheral InterventionCompletedNCT03044002
• ProMRI ICD/CRT-D Post Approval StudyCompletedNCT02933619
• Safety and Clinical Performance of a Sirolimus-eluting Absorbable Metal ScaffoldSuspendedNCT02916485Not applicable
• BIOLUX P-IV CHINA ( BIOTRONIK )CompletedNCT02912715Not applicable

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