| Recruiting | BIOTRONIK Investigation of the LivIQ Leadless Pacemaker System Leadless Pacemaker, Bradycardia, AV Block | N/A | 2026-03-16 |
| Active Not Recruiting | BIOTRONIK Conduction System Pacing With the Solia Lead - Solia CSP S Sinus Node Dysfunction, Bradycardia, Atrioventricular Block | N/A | 2024-12-18 |
| Completed | BIOTRONIK Conduction System Pacing With the Solia Lead Bradycardia, Atrioventricular Block, Left Bundle-Branch Block | N/A | 2022-12-12 |
| Active Not Recruiting | A First in Human Feasibility Study to Evaluate the Safety and Effectiveness of the BIOTRONIK Prospera SCS Syst Chronic Low-back Pain, Chronic Leg Pain | N/A | 2021-09-20 |
| Terminated | Atrial Fibrillation Associated With Heart Failure Treated by BIOTRONIK's CRT-DX System Heart Failure, Atrial Fibrillation, Cardiac Resynchronization Therapy | — | 2021-05-28 |
| Completed | Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Arter Coronary Artery Disease, Atherosclerosis, Coronary, Myocardial Ischemia | — | 2020-01-24 |
| Terminated | Assessment of the Utility of BIOMONITOR to Identify Atrial Fibrillation (AF) in Ablation Candidates Using Prec Atrial Fibrillation | — | 2019-09-25 |
| Completed | Analysis of Both Sex and Device Specific Factors on Outcomes in Patients with Non-Ischemic Cardiomyopathy Cardiomyopathies, Gender, Implantable Defibrillator User | — | 2019-05-09 |
| Completed | Comparison of the Effects of Two Spinal Cord Stimulation (SCS) Therapies on Subject Reported Pain (BENEFIT-02) Chronic Low Back Pain, Chronic Leg Pain | N/A | 2018-08-01 |
| Completed | QP ExCELs: MultiPole Pacing (MPP) Sub-Study Heart Failure | N/A | 2017-05-19 |
| Terminated | Plexa ICD Lead Registry Implantable Defibrillator User | — | 2017-05-18 |
| Completed | ProMRI ICD/CRT-D Post Approval Study Tachyarrhythmia | — | 2016-08-01 |
| Completed | BioMonitor 2 In-Office Setting Insertion Safety and Feasibility Evaluation With Device Functionality Assessmen Insertable Cardiac Monitor | — | 2016-06-01 |
| Completed | Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Arter Coronary Artery Disease, Atherosclerosis, Coronary, Myocardial Ischemia | N/A | 2015-05-01 |
| Terminated | Protego DF4 Post Approval Registry Implantable Defibrillator User | — | 2014-09-27 |
| Completed | ProMRI Study of the Iforia ICD System (Phase C) Implantable Cardioverter-Defibrillator With Magnetic Resonance Imaging | — | 2014-06-01 |
| Completed | ProMRI Study of the Entovis Pacemaker System (Phase B) Magnetic Resonance Imaging (MRI); Cardiac Pacing | — | 2013-12-01 |
| Terminated | Safety and Performance Study of the Siello S Pacing Lead Safety and Effectiveness of the Siello S Lead | — | 2013-03-13 |
| Completed | ProMRI Study of the Entovis Pacemaker System Safety of the ProMRI Pacemaker System Under Specific MRI Conditions | — | 2013-02-01 |
| Completed | BIOHELIX-I Bare Metal Stent Study Coronary Arteries Disease | Phase 2 / Phase 3 | 2012-11-01 |
| Completed | Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents Peripheral Artery Disease, Peripheral Vascular Disease | Phase 2 | 2011-07-01 |
| Completed | Post Approval Registry of Corox OTW, Endocardial, Left Ventricular Steroid Lead, Bipolar Congestive Heart Failure | — | 2008-12-01 |
| Completed | Long-term Evaluation of the Linox Family ICD Leads Registry (GALAXY) Patients Indicated for an ICD | — | 2008-12-01 |
| Terminated | Echocardiography Guided Cardiac Resynchronization Therapy (EchoCRT) Heart Failure, Ventricular Dyssynchrony | Phase 2 / Phase 3 | 2008-08-01 |
| Terminated | Combined Use of BIOTRONIK Home Monitoring and Predefined Anticoagulation to Reduce Stroke Risk Atrial Fibrillation, Atrial Flutter, Stroke | Phase 4 | 2008-02-01 |
| Completed | Interventricular Delay of Lumax HF-T for Heart Failure Congestive Heart Failure | Phase 2 | 2007-07-01 |
| Completed | REPLACE: Implantable Cardiac Pulse Generator Replacement Registry Device Replacement, Elective Replacement (ERI), Device Advisory | — | 2007-07-01 |
| Completed | TRIAGE-CRT Telemonitoring in Patients With CHF and Indication of CRT-D Congestive Heart Failure, Cardiac Resynchronization Therapy | Phase 4 | 2006-11-01 |
| Completed | COSMO Post Approval Registry: Corox OTW Steroid LV Lead Monitoring Congestive Heart Failure | Phase 4 | 2006-10-01 |
| Completed | Effectiveness of Pacemaker With Closed Loop Stimulation Compared to Pacemakers With and Without Standard Rate Bradycardia | Phase 4 | 2006-05-01 |
| Completed | TRUST: Lumos-T Safely RedUceS RouTine Office Device Follow-up Patient Indicated for an ICD | Phase 4 | 2005-11-01 |
| Terminated | Investigational Device Exemption (IDE) Study for the Approval of Closed Loop Stimulation (CLS) and Cardiac Res Atrial Fibrillation, Congestive Heart Failure | N/A | 2004-12-01 |