Boston Scientific Corporation: all 611 studies
Page 5 of 7. Open to participants first (44), then studies with results posted, then the rest; newest registration first within each.
- ACURATE neo2™ Post Market Clinical Follow up StudyActive, not recruitingNCT04655248
- SpyGlass™ Discover PercutaneousCompletedNCT04580940
- Spinal Cord Stimulation in the Treatment of Chronic, Intractable Pain Using the Nalu™ Neurostimulation SystemCompletedNCT04503109Not applicable
- The Intracept Global Registry ( TIGR ) - Pilot StudyTerminatedNCT04449835
- CHAMPION-AF Clinical TrialActive, not recruitingNCT04394546Not applicable
- I Can sEe Left Atrial Appendage (ICELAA) Clinical StudyCompletedNCT04196335Not applicable
- A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)Active, not recruitingNCT04192591Not applicable
- A Feasibility Study of the Millipede Transcatheter Annuloplasty Ring System in Patients With Functional Mitral RegurgitationActive, not recruitingNCT04147884Not applicable
- Physiological Signals, Activity and Posture for Surface Mounted Insertable Cardiac Monitor in Heart Failure StudyCompletedNCT04112576
- An "All-Comers" Study of the AgentTM MONORAILTM Paclitaxel-Coated PTCA Balloon Catheter Used in Real-World Clinical Practice in Chinese PatientsCompletedNCT04085445
- Non-Interventional Registry Study to Evaluate the Effectiveness of TheraSphere® in the Treatment of Hepatocellular Carcinoma (HCC)CompletedNCT04069468
- Registry Study to Evaluate the Performance and Safety of Roxwood Medical Catheters in Arteries of Participants With a Stenotic Lesion or Chronic Total Occlusion (CTO)WithdrawnNCT04059536
- RESPOND EDGE Post Market StudyTerminatedNCT04009720
- The ENROUTE Transcarotid Neuroprotection System (ENROUTE Transcarotid NPS) DW-MRI StudyCompletedNCT03985774
- A Clinical Trial to Confirm Safety & Effectiveness of the SYNERGY 4.50 mm and 5.00 mm Stent for Treatment of Atherosclerotic Lesion(s)CompletedNCT03875651
- Boston Scientific's Single Shot LUMINIZE RF Balloon Catheter in the Treatment of Symptomatic, Drug Refractory Paroxysmal Atrial FibrillationWithdrawnNCT03852420Not applicable
- WATCHMAN for Concomitant Left Atrial Appendage Electrical Isolation and Occlusion to Treat Persistent Atrial Fibrillation RhythmWithdrawnNCT03835338Not applicable
- Cardiac Monitor Employee StudyCompletedNCT03826225
- AXIOS CHINA (E7148)CompletedNCT03808272Not applicable
- Hot AXIOS System Japan Post Market SurveyCompletedNCT03797209
- Cholangioscopy in Primary Sclerosing Cholangitis (PSC)CompletedNCT03766035
- ACURATE TF™ Transfemoral Aortic Bioprosthesis for Implantation in Patients With Severe Aortic Stenosis (2011-03)CompletedNCT03752996Not applicable
- China Greenlight Registry Study (Post-market)CompletedNCT03736512
- A Post-Approval, Single-Arm Study of the SYNERGY Stent System in ChinaActive, not recruitingNCT03736226
- Coordinated Reset Deep Brain StimulationCompletedNCT03732898Not applicable
- Intra-operative Pancreatoscopy in Patients With IPMNActive, not recruitingNCT03729453
- Data Collection - Of Syncope Tilt Table Testing StudyCompletedNCT03721393
- Initial Case Series With Exalt Single-Use DuodenoscopeCompletedNCT03701958Not applicable
- Intraosseous Basivertebral Nerve Ablation for Treatment of Chronic Low Back PainWithdrawnNCT03658018Not applicable
- Data Collection Atrial Fibrillation Exploratory StudyTerminatedNCT03647085
- Intraosseous Basivertebral Nerve Ablation for the Treatment of Chronic Low Back PainWithdrawnNCT03630133Not applicable
- Multi-center Complex Atrial Tachycardia High-Resolution Mapping Registry (MATH)WithdrawnNCT03613831
- Precision Event Monitoring for Patients With Heart Failure Using HeartLogicCompletedNCT03579641
- Feasibility Trial on ACURATE™ Transapical Implantation in Patients With Severe Symptomatic Aortic Stenosis (2009-01)CompletedNCT03567278Not applicable
- RadioEmbolization for the ADvancement of Y90 Glass Microspheres RegistryTerminatedNCT03516695
- CHANGE Neo™ TA Registry With ACURATE Neo™ Aortic Bioprosthesis and ACURATE Neo™ TA Transapical Delivery SystemTerminatedNCT03454360
- Study in the Treatment of HCC With a Radiopaque (RO) Bead (LC Bead LUMI™) Loaded With DoxorubicinWithdrawnNCT03452553Not applicable
- A TheraSphere® Advanced Dosimetry Retrospective Global Study in HCCCompletedNCT03295006
- Chronic Obstructive Pulmonary Disease (COPD) Co-Pilot AIR Substudy of CLN0014TerminatedNCT03267992
- Bronchial Thermoplasty 10+ Year StudyCompletedNCT03243292
- POCS in Liver Transplantation PatientsCompletedNCT03205072
- ACURATE TA™ Valve Implantation: SAVI Registry (Surveillance Plan #2011-02) (TA-SAVI)CompletedNCT03143686
- ACURATE™ Transapical Aortic Bioprosthesis for Implantation in Patients With Severe Aortic Stenosis (2010-01)CompletedNCT03143673Not applicable
- REPRISE China - Clinical Evaluation in ChinaWithdrawnNCT03084510Not applicable
- Assessing Superion Clinical Endpoints vs. DecompressionWithdrawnNCT03048955Not applicable
- Performance and Safety of the Lotus™ Valve With a FLEXible Delivery SystemCompletedNCT03043404Not applicable
- ACURATE TF™ Transfemoral Aortic Bioprosthesis for Implantation in Patients With Severe Aortic Stenosis:CE-approval CohortCompletedNCT03003650Not applicable
- PRospective Observation of Aortic reGuRgitation aftEr TAVI and progreSS Over Time: PROGRESS PVL RegistryCompletedNCT02987894
- ACURATE Neo™ Aortic Bioprosthesis for Implantation Using the ACURATE TA™ LP Transapical Delivery System in Patients With Severe Aortic StenosisCompletedNCT02986737Not applicable
- REPRISE EDGE 29 mm EU StudyWithdrawnNCT02964962Not applicable
- ACURATE Neo™ TA Delivery System in Patient With Severe Aortic StenosisCompletedNCT02950428Not applicable
- ACURATE Neo™ AS Aortic Bioprosthesis for Implantation Using the ACURATE neoTM AS TF Transfemoral Delivery System in Patients With Severe Aortic StenosisCompletedNCT02909556Not applicable
- REpositionable Percutaneous Replacement of NatIve StEnotic Aortic Valve Through Implantation of LOTUS EDGE Valve SystemTerminatedNCT02854319Not applicable
- ChOcolate COnsumption And Blood Pressure (COCOA-BP): A Wearable Devices Pilot TrialCompletedNCT02764203Not applicable
- Prospective Registry on User Experience With The Mapping System For Ablation ProceduresCompletedNCT02698670
- ACURATE TA™ Valve Implantation Registry: SAVI 2CompletedNCT02663375
- Watchman FLX Left Atrial Appendage Closure Device Post Approval Study ( Europe Only)CompletedNCT02654470
- Exploratory Study of Upper and Lower Endoscopic Fuse SystemCompletedNCT02651857Not applicable
- Vela China Study: in Cutting And Hemostasis For Gastrointestinal Epithelial Neoplasia In Chinese PopulationTerminatedNCT02636738Not applicable
- Treatment of REfractory Overactive BLadder With the AXonics Sacral Neuromodulation System (RELAX-OAB)CompletedNCT02620410Not applicable
- Annular Reshaping of the Mitral Valve for Patients With Mitral Regurgitation Using the Millipede IRIS SystemCompletedNCT02607527Not applicable
- Safety and Efficacy Study of Lotus Valve for Transcatheter Aortic Valve Replacement (REPRISE Japan)CompletedNCT02491255Not applicable
- The Captivator EMR RegistryCompletedNCT02482701
- Study of Intraparenchymal Therapy With Irinotecan Drug Eluting Beads as Adjunct to Recurrent Surgically Resectable High Grade GliomaTerminatedNCT02481960Phase 1/2
- FAST Feasibility StudyCompletedNCT02470884Not applicable
- EndoChoice's Fuse® Endoscopic System Performance In Routine PracticeCompletedNCT02439502Phase 4
- Study of Intraparenchymal Therapy as Adjunct Therapy in Patients With Recurrent, Resectable Glioblastoma Multiforme.TerminatedNCT02433392Phase 1
- REPRISE Next Generation Delivery SystemCompletedNCT02329496Not applicable
- Symetis ACURATE Neo™ Valve Implantation SAVI TF RegistryCompletedNCT02306226
- SpyGlass Direct Visualization System Clinical Registry in ChinaCompletedNCT02287194
- SpyGlass AMEA RegistryCompletedNCT02281019
- Short Term Pancreatic Stenting RegistryCompletedNCT02262845
- Prospective, Multi-Center All-Comer Biliary Canadian WallFlex RegistryCompletedNCT02261623
- Sentinel(TM) Post-Market RegistryCompletedNCT02255851
- BodyGuardian Respiration and Activity Validation TestingCompletedNCT02255526
- A Study of EndoChoice's Upper&Lower Endoscopic Systems Utilizing a Full Spectrum Optical TechnologyCompletedNCT02143284Not applicable
- Pancreatic Metal Stents in Chronic PancreatitisCompletedNCT02135809Not applicable
- Bronchial Thermoplasty Global RegistryCompletedNCT02104856
- LONGEVITY Study. Evaluation of the Device and Battery Longevity of Boston Scientific Market-released ICD and CRT-D DevicesCompletedNCT02091011
- Treatment of Resistant Hypertension by Renal Denervation in ChinaTerminatedNCT02027012Not applicable
- Registry on WATCHMAN Outcomes in Real-Life Utilization WASP RegistryCompletedNCT01972295
- MICHI™ Neuroprotection System (NPS+f) Filter Debris Analysis Study (The F-1 Study)CompletedNCT01877174
- MADIT ASIA Cardiac Resynchronization TrialTerminatedNCT01872234Phase 3
- Post Market Observational, Prospective, Multi-center StudyTerminatedNCT01806636
- Signal Transfer of Atrial Fibrillation Data to Guide Human TreatmentCompletedNCT01765075
- IntellaTip MiFi XP Ablation Catheter TrialCompletedNCT01730807Not applicable
- Clinical Outcome of Pacemaker paTIents According to Pacing Modality and Primary INDications OPTI-MIND 2CompletedNCT01715558
- Post-Approval Study of PROMUS Element™ in ChinaCompletedNCT01677585
- Electroanatomical Mapping of Patients Undergoing Catheter Ablation Procedures Using Rhythmia Mapping System and CatheterCompletedNCT01642537Not applicable
- ELEVATE (Evaluation of Left Ventricular Autothreshold) 3.0CompletedNCT01539629
- Carotid Filtration During Endovascular Aortic Valve ImplantationCompletedNCT01484249Not applicable
- Safety and Efficacy of Cryoablation for the Palliation of Painful Bone MetastasesCompletedNCT01461265Phase 1
- Safety and Efficacy of Cryoablation Combined With Radiation Therapy for the Palliation of Painful Bone MetastasesWithdrawnNCT01461252Phase 1
- The ACE Follow-up StudyCompletedNCT01429194Not applicable
- Evaluation of Physiologic Parameters to Study the Mechanism of Action of the Lung Volume Reduction Coil in Subjects With Homogeneous EmphysemaCompletedNCT01421082Phase 2/3
- Safety and Efficacy of Cryoablation for Abdominal Pain Associated With Pancreatic CancerTerminatedNCT01335945Phase 1
- Randomized Comparison of the RePneu Lung Volume Reduction Coil (LVRC) to Standard of Care for the Treatment of Emphysema (RESET Study)CompletedNCT01334307Phase 1
- Feasibility Study of PneumRx's Lung Volume Reduction Coil (LVRC)CompletedNCT01328899Phase 1/2
- High Septal Pacing for Cardiac Resynchronization TherapyTerminatedNCT01325480
- Study of Cytrix Use in Pelvic Floor Prolapse TreatmentCompletedNCT01244165Phase 4