Medtronic: all 1,087 studies
Page 9 of 11. Open to participants first (56), then studies with results posted, then the rest; newest registration first within each.
- French Post-Inscription Study on Sacral Neuromodulation in the Treatment of Fecal IncontinenceCompletedNCT01957969
- REVEAL for Respiration DetectionStatus unknownNCT01956578Not applicable
- MDT-2113 Drug-Eluting Balloon vs. Standard PTA for the Treatment of Atherosclerotic Lesions in the Superficial Femoral Artery and/or Proximal Popliteal ArteryCompletedNCT01947478Not applicable
- Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot StudyCompletedNCT01944228Phase 1
- Rapid Renal Sympathetic Denervation for Resistant Hypertension IIWithdrawnNCT01939392Phase 2/3
- A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in Subjects With Lumbosacral RadiculopathyCompletedNCT01917825Phase 2
- Respiration Rate Monitoring During TransitionsCompletedNCT01881269
- Epilepsy Motion SensingCompletedNCT01850498
- OneShot Renal Denervation RegistryTerminatedNCT01844037Phase 2/3
- Gastric Electrical Stimulation (GES) for the Treatment of ObesityCompletedNCT01823705Not applicable
- Feasibility Study of Remote Support for Implantable Pulse Generator (IPG)/Implantable Cardioverter Defibrillator (ICD) ImplantCompletedNCT01809652Not applicable
- Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Paroxysmal Atrial FibrillationCompletedNCT01803438Phase 4
- Integrated Diagnostic for Heart FailureCompletedNCT01798797
- Pulse Oximetry_Performance Testing- PCBA-1 (Printed Circuit Board Assembly) NEO/PEDSCompletedNCT01797250
- Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIic)CompletedNCT01793376
- Pulse Oximetry- Evaluating Resp Rate- PCBA-1CompletedNCT01791582
- Pulse Oximetry- Evaluating Sensor Off- PCBA-1CompletedNCT01791569
- Development of Applications of the Bravo® pH Monitoring System and Evaluation of Its Performance (Encore)WithdrawnNCT01788085Not applicable
- Collection of Performance Data From the Integrated Sensor and Infusion Set. TRIAL 4Status unknownNCT01775059Not applicable
- Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment of Descending Thoracic Aortic Diseases (VALIANT CAPTIVIA France)CompletedNCT01775046
- Feasibility Study - Integrated Sensor and Infusion Set. Trial IIICompletedNCT01773668Not applicable
- Feasibility Study of an Integrated Sensor and Infusion SetCompletedNCT01770561Not applicable
- PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter (PVAC GOLD)CompletedNCT01767558Not applicable
- Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV)CompletedNCT01762124Not applicable
- Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed Circuit Board Assembly)CompletedNCT01747473
- Pulse Oximetry_Performance Testing- PCBA-1 (Printed Circuit Board Assembly)CompletedNCT01747460
- Bipolar Sealer Aquamantys Use in Total Knee ReplacementCompletedNCT01736644Not applicable
- PANORAMA 2 Observational StudyCompletedNCT01723566
- Pulse Oximetry- Performance During Severe Signal InterferenceCompletedNCT01720355
- Enable® Aortic Sutureless Bioprosthesis EvaluationCompletedNCT01720342
- Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Glucose Levels During an Overnight PeriodCompletedNCT01712594Not applicable
- Multi-electrode Radiofrequency Renal Denervation System Feasibility StudyCompletedNCT01699529Not applicable
- Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptomatic Severe Aortic Stenosis With Significant Comorbidities in Extreme Risk Subjects Who Need Aortic Valve ReplacementCompletedNCT01675440
- The Product Surveillance Registry REVERSE Post Approval StudyCompletedNCT01660035
- Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of Paroxysmal Atrial FibrillationCompletedNCT01645917Phase 4
- Renal Denervation by MDT-2211 System in Patients With Uncontrolled HypertensionCompletedNCT01644604Not applicable
- DF4 Connector System Post-Approval StudyCompletedNCT01638897
- Enable I Long-term Follow-up StudyTerminatedNCT01636648
- Sagittal Plane Correction With Pass-LP Device in Adult Deformity PatientsCompletedNCT01635322
- Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncontrolled HyperTensioN in IndiaTerminatedNCT01632943Not applicable
- Medtronic Market-Released DF4 Lead ImagingCompletedNCT01626768
- Cutaneous Heart Sounds Data Collection During Cardiac Resynchronization Therapy (CRT) Optimization StudyCompletedNCT01609985
- The Sapheon Closure System Feasibility StudyCompletedNCT01603433Not applicable
- Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule EndoscopyCompletedNCT01575093Phase 1/2
- Post-Approval Study for the MOSAIC® BioprosthesesCompletedNCT01574625
- European Sapheon™ Closure System Observational ProspectivE (eSCOPE) StudyCompletedNCT01570101Not applicable
- Registry AutoLog Lipid Removal and Blood Component CharacterizationCompletedNCT01565967
- UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Implantable Cardiac Defibrillator (ICD) ImplantTerminatedNCT01561144
- International Retrospective Study of Pipeline Embolization DeviceCompletedNCT01558102
- Aneurysm Study of Pipeline in an Observational RegistryTerminatedNCT01557036
- Stable Angina Observational RegistryCompletedNCT01552109
- Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients With Chagas DiseaseTerminatedNCT01539161Phase 4
- ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registry)CompletedNCT01534819
- Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic Aneurysms (ENDURANT France)CompletedNCT01526811
- Product Surveillance Registry- Deep Brain Stimulation for EpilepsyCompletedNCT01521754
- GRANVIA®-C Cervical Disc Prosthesis Multicenter European Pilot StudyCompletedNCT01518582
- Impedance Measurements in Heart Failure PatientsTerminatedNCT01509495Phase 1
- 4P Study: Predictive Quality With Painfree TherapiesCompletedNCT01509378
- Development of Applications of the Bravo® pH Monitoring System and Evaluation of Its PerformanceCompletedNCT01503476Phase 4
- Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instability Requiring Surgical FusionCompletedNCT01495234Not applicable
- Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseTerminatedNCT01494493Not applicable
- Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01494454Not applicable
- Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01494441Not applicable
- A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01494428Not applicable
- rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level)CompletedNCT01491568Not applicable
- INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot StudyCompletedNCT01491542Not applicable
- TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot StudyCompletedNCT01491516Not applicable
- INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical Plate System Pivotal TrialTerminatedNCT01491477Not applicable
- A Pivotal Study of rhBMP-2/ACS/INTER FIX™ Device for Posterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseTerminatedNCT01491464Not applicable
- A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491451Not applicable
- A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491425Not applicable
- INFUSE™ BONE GRAFT/CORNERSTONE-SR™ Allograft Ring/ATLANTIS™ Anterior Cervical Plate- Pilot StudyCompletedNCT01491399Not applicable
- Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01491386Not applicable
- Pilot Study of rhBMP-2/ACS/LT-CAGE® for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491373Not applicable
- Acute Carotid Sinus Endovascular Stimulation II StudyCompletedNCT01458483Phase 1
- Evaluation of PillCam With Blood-Sensing Feature: A Feasibility StudyTerminatedNCT01448382Phase 1
- ReStore Thrombectomy Trial for Flow Restoration in Acute Ischemic Stroke PatientsSuspendedNCT01437774Not applicable
- Medtronic South Asian Systolic Heart Failure RegistryCompletedNCT01434615Phase 4
- SYMPLICITY HTN-3 Renal Denervation in Patients With Uncontrolled HypertensionCompletedNCT01418261Not applicable
- Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast ReductionWithdrawnNCT01404351Not applicable
- Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Clinical TrialTerminatedNCT01392196Not applicable
- Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System for Colon Cleansing EnhancementTerminatedNCT01370759Phase 1
- Diabetes Multicenter Observational Study (DIAMOND-1-)Status unknownNCT01369823
- Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial DiseaseCompletedNCT01366482Not applicable
- Model 20066 Left Ventricular (LV) Lead StudyCompletedNCT01365234Phase 1
- Characterization of Interventricular Conduction MeasurementsCompletedNCT01362465Early Phase 1
- Model 4396 Left Ventricular (LV) Lead Chronic Performance StudyCompletedNCT01361685
- Model 4296 Left Ventricular (LV) Lead Chronic Performance StudyCompletedNCT01361672
- Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Implantation System - The Engager European Pivotal TrialCompletedNCT01348438Not applicable
- Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections StudyTerminatedNCT01341483
- RESOLUTE China RCTCompletedNCT01334268Not applicable
- Salient Aquamantys Spine TrialTerminatedNCT01331499Phase 4
- Effectiveness Study of the Guardian RT in Type 1 DiabeticsCompletedNCT01331343Phase 4
- Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter StudyCompletedNCT01323439
- Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vertical Ridge AugmentationWithdrawnNCT01308996Not applicable
- SureScan Post-Approval StudyCompletedNCT01299675
- The STAPLE International Post-Market RegistryTerminatedNCT01276249
- Evaluation of Gastric Juice Samples During Standard Gastroscopy ProcedureTerminatedNCT01267318
- ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up TrialTerminatedNCT01264484
- RESOLUTE China Registry:CompletedNCT01243749