Medtronic: all 1,087 studies
Page 7 of 11. Open to participants first (56), then studies with results posted, then the rest; newest registration first within each.
- Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Lead in Patients With ICD or CRT-DActive, not recruitingNCT06745778
- SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Patients With Type 1 and Type 2 DiabetesWithdrawnNCT06719531Not applicable
- AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Undergoing Ventral Hernia RepairActive, not recruitingNCT06710795Not applicable
- Product Surveillance Registry; Ear, Nose and Throat - EXTEND CohortWithdrawnNCT06671561
- OM2 Low Saturation VerificationCompletedNCT06661889
- Smart MDI Study (CIP343)CompletedNCT06645834Not applicable
- Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Continuous Vitals Monitoring - Department of Anesthesia at PHCActive, not recruitingNCT06638073
- Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital CohortCompletedNCT06637995
- Pulse Oximetry Performance Comparison in NewbornsCompletedNCT06637917
- Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing (The CORE-CPP Study)Active, not recruitingNCT06606288
- Safety Evaluation of MiniMed™ 780G System With DS5 CGM in ChildrenCompletedNCT06604871Not applicable
- Perfusion Index ParameterCompletedNCT06586918
- Accuracy Performance Verification of the INVOS™ PM7100 System in AdultsCompletedNCT06581835
- Bolt CSP-M Holter StudyActive, not recruitingNCT06540521
- Avalus Ultra Post-Approval Study (PAS)Active, not recruitingNCT06506903Not applicable
- Electrically Evoked Compound Action Potentials Human Observation Medtronic System Study (ECHO-MDT)CompletedNCT06499220Not applicable
- Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral HerniaActive, not recruitingNCT06449378Not applicable
- OM2 Abbreviated Sensor VerificationCompletedNCT06415799
- OM2 Motion Verification StudyCompletedNCT06415786
- CLIP-IT Post-Market StudyActive, not recruitingNCT06203054Not applicable
- Enlighten Study: The EV-ICD Post Approval RegistryActive, not recruitingNCT06048731
- Affera Global RegistryActive, not recruitingNCT06026345
- Accuracy Performance Verification of the INVOS™ System in PediatricsCompletedNCT05962905
- Propel Drug-Eluting Sinus Stent Family Open CohortCompletedNCT05925985
- Advancing Cath Lab Results With FFRangio Coronary Physiology AssessmentActive, not recruitingNCT05893498Not applicable
- Fast Induced Remodeling in Heart Failure With Preserved Ejection FractionActive, not recruitingNCT05839730Not applicable
- Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal Cord Stimulation (SCS) Modalities for Chronic PainTerminatedNCT05775510
- Allometric-Pace StudyCompletedNCT05766462
- N600X Low Saturation Accuracy ValidationCompletedNCT05532670
- The MONARCH Case Series Study: SPRINT® Peripheral Nerve Stimulation for the Treatment of Head PainActive, not recruitingNCT05491915Not applicable
- Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enteroscopy Routine Care Procedures (GPS Study)WithdrawnNCT05450393
- Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of Incisional Hernia OccurrenceActive, not recruitingNCT05424484Not applicable
- TYRX™ Pocket Health StudyCompletedNCT05356546
- DIAMOND AF Post-Approval StudyTerminatedNCT05230524
- STOP AF First Post-Approval StudyCompletedNCT05227053
- SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subjects With Uncontrolled HTNActive, not recruitingNCT05198674Not applicable
- Evolut™ EXPAND TAVR II Pivotal TrialActive, not recruitingNCT05149755Not applicable
- Harmony TPV Post-Approval StudyActive, not recruitingNCT05077774Not applicable
- INSPIRE Pipeline™ Shield Post Approval StudyActive, not recruitingNCT05071963
- Cardiac Implantable Electronic Device (CIED) Research StudyActive, not recruitingNCT05061862
- ExtraVascular Implantable Cardiac Defibrillator Continued Access StudyWithdrawnNCT05049720Not applicable
- InPen User ExperienceCompletedNCT05029271Not applicable
- Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated With Neurothrombectomy Devices in IndiaCompletedNCT05005962
- STOP Persistent AF PASActive, not recruitingNCT05005949
- Solitaire Aneurysm Remodeling RegistryWithdrawnNCT04905303
- Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility StudyCompletedNCT04873271Not applicable
- Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation for Defibrillation and Reliability in Left Bundle Branch Area Pacing (LEADR LBBAP)CompletedNCT04863664Not applicable
- HVAD(TM) SMART 1.0 StudyWithdrawnNCT04854200
- SpO2 Accuracy Low Saturation Validation of the OxySoftN SensorCompletedNCT04811963
- PLASMA Chile (PLASMA Chile)CompletedNCT04757142
- Electrogram and Hemodynamic Characteristics of Adaptive LBBAP in Patients With Heart Failure or BradycardiaCompletedNCT04738396
- DiamondTemp Global RegistryActive, not recruitingNCT04735016
- Medtronic PSR TDD PMCFCompletedNCT04714385
- Chronic Obstructive Pulmonary Disease (COPD) MonitoringStatus unknownNCT04671888Not applicable
- European CURE-AF StudyCompletedNCT04645615Not applicable
- IN.PACT™ Quality of Life Post-Reimbursement StudyActive, not recruitingNCT04597307
- SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion StudyCompletedNCT04559763
- Prospective Clinical Study to Evaluate the Efficacy of the Stand-alone Cervical Interbody Cage C-CURVE ( Titanium) Manufactured by MEDICREA®CompletedNCT04547959Not applicable
- Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS)CompletedNCT04543747
- IN.PACT™ AV Access Post-Approval Study (PAS002)Active, not recruitingNCT04543539
- Reveal LINQ Respiration Clinical StudyCompletedNCT04506684
- Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Study (iATP PAS)Active, not recruitingNCT04496518
- AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy SystemTerminatedNCT04494035Not applicable
- Personalized Therapy Study - HFRS (TriageHF) Post Approval StudyActive, not recruitingNCT04489225
- TTVR Early Feasibility StudyActive, not recruitingNCT04433065Not applicable
- Flow Arrest Safety and Technical Success With Balloon Guide CathetersCompletedNCT04416659
- Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System for Subacute and Chronic Subdural HematomaCompletedNCT04402632Not applicable
- EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysms With the Pipeline™ Flex Embolization Device With Shield TEchnology™ (ELEVATE)TerminatedNCT04391803Not applicable
- Pivotal Study of the Medtronic Axys EX Rotational Atherectomy SystemWithdrawnNCT04282161Not applicable
- DISSECT-N Post Market Data Collection RegistryCompletedNCT04267055
- Micra AV Transcatheter Pacing System Post-Approval RegistryCompletedNCT04253184
- The RESET Clinical Trial: SPRINT® Peripheral Nerve Stimulation for the Treatment of Back PainCompletedNCT04246281Not applicable
- Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pacemakers (Micra AV CED)Active, not recruitingNCT04235491
- PLASMA Mexico (PLASMA Mexico)CompletedNCT04214899
- Image Location and Performance of Left Bundle Branch PacingCompletedNCT04119323
- Transforaminal Lumbar Interbody Fusion (TLIF)Active, not recruitingNCT04073563Not applicable
- Apogee InternationalTerminatedNCT04065997
- Personalized Therapy Study - Attain Stability Quad Post-Approval StudyActive, not recruitingNCT04024943
- Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Branches Area in Pacing-indicated PatientsCompletedNCT04023890
- SelectSecure 3830 Lead ImagingCompletedNCT03941275
- Titan Spine Endoskeleton TT/TO StudyTerminatedNCT03910309
- Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study (EPAS)TerminatedNCT03900468Not applicable
- MDT-1118 Japan DT StudyCompletedNCT03884504Phase 3
- CAPERE Thrombectomy System Post-Market Clinical Follow Up StudyTerminatedNCT03869645
- Personalized Spine Study Group RegistryWithdrawnNCT03843476
- Implantable System for Remodulin Post-Approval StudyWithdrawnNCT03833323
- Definition and Validation of Normative Data of EndoFLIP™ Measurements in Healthy SubjectsWithdrawnNCT03831724Not applicable
- Connected Pens for Diabetes StudyTerminatedNCT03830216Not applicable
- Diffusion MRI-1 Imaging DatabaseCompletedNCT03775694
- Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Developments (SODA)CompletedNCT03771508
- Personalized CRT - PSRCompletedNCT03723265
- FIRE AND ICE II Trial PilotCompletedNCT03706677Not applicable
- Destination Therapy Post Approval StudyActive, not recruitingNCT03681210
- Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ System for Fast Treatment of Patients With Atrial FibrillationCompletedNCT03626649Not applicable
- O-arm Assessment of Vertebral Movement Using ST2R TechniqueWithdrawnNCT03609138
- Trending of Respiratory Rate Using the Nellcor™ Bedside Respiratory Patient Monitoring SystemCompletedNCT03593603
- CT Data Collection StudyCompletedNCT03589664
- Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Patients in Operating RoomCompletedNCT03553953
- Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase TacksCompletedNCT03526341
- A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast Lesion Excision System (BLES)TerminatedNCT03520127