MicroPort Scientific Corporation: all 121 studies
Page 1 of 2. Open to participants first (41), then studies with results posted, then the rest; newest registration first within each.
- CardioFlow Transcatheter Mitral Valve Replacement System Pre-market Clinical InvestigationNot yet recruitingNCT07857343Not applicable
- PulseMagic™ TrueForce™ PAF NMPA StudyNot yet recruitingNCT07720557Not applicable
- Coronary Laser Atherectomy System for Treatment of Coronary Artery Stenosis (SHINE)Not yet recruitingNCT07697638Not applicable
- Post-market European & Asian Registry to Evaluate the Minos™ Stent-Graft and Delivery System in Abdominal Aortic Aneurysm TreatmentRecruitingNCT07674173
- European Multi-Centre Post-Market Registry on Thoracic Endovascular Arch Repair Using Castor™ and Cratos™RecruitingNCT07668687
- CHU Dual-Energy Ablation in Ventricular ArrhythmiaEnrolling by invitationNCT07503769Not applicable
- The Coronary Sinus Balloon Pump in STEMINot yet recruitingNCT07354035Not applicable
- Safety and Performances of the LINEA Cardiac Pacing Lead Optimized for the Implantation in Interventricular SeptumRecruitingNCT07342608Not applicable
- The Liquid Embolic Agent for the Treatment of Brain Arteriovenous MalformationRecruitingNCT07314047Not applicable
- Left Bundle Branch Area Pacing (LBBAP) Monitoring Assistant: Evaluation of Portable ECG SolutionRecruitingNCT07254013Not applicable
- Prospective, Multicenter, Single-Arm Study of Aortic Arch Pathology ReconstructionNot yet recruitingNCT07139912Not applicable
- The First-In-Man Use of Coronary Sinus Balloon Pump in STEMI Patients Treated by Primary PCINot yet recruitingNCT07082153Not applicable
- Clinical Study on the Efficiency of Rapid Arrhythmia Mapping Using EasyStars™ High Density Mapping Catheter ApplicationsNot yet recruitingNCT07079813Not applicable
- Clinical Study on the Safety and Efficacy of a New Magnetic Navigation Radiofrequency Ablation Catheter for Rapid ArrhythmiaNot yet recruitingNCT07067372Not applicable
- A Clinical Study on the Use of a Domestically Produced Three-dimensional Cardiac Electrophysiological Mapping System Combined With Pressure Monitoring Technology and Star Mapping Technology for the Treatment of Paroxysmal Atrial Fibrillation.Not yet recruitingNCT07039032Not applicable
- A Clinical Study on the Use of a Domestically Produced Cryoablation System Combined With Balloon Cryoablation Technology for the Treatment of Paroxysmal Atrial FibrillationNot yet recruitingNCT07036068Not applicable
- Safety and Efficacy Study of the First Domestically Produced FireMagic™ PreciSense™ 3D Microelectrode Ablation Catheter Therapy for Rapid Arrhythmia With Tissue Temperature Measurement FunctionNot yet recruitingNCT07032948Not applicable
- A Randomized Trial of the Rapamycin Target Eluting Stent for the Treatment of Symptomatic Cerebral Artery Atherosclerotic Disease（TARGET-DREAM）Not yet recruitingNCT06925971Phase 3
- A PILOT TRIAL of a DISPOSABLE INTRACEREBRAL ASPIRATION ENDOSCOPE for the TREATMENT of INTRACEREBRAL HEMATOMA（FAST-HET）RecruitingNCT06843616Not applicable
- Registration Trial of the Drug-coated Balloon for the Symptomatic Cerebral Atherosclerotic StenosisEnrolling by invitationNCT06683118Not applicable
- TAVR vs. SAVR Study of VitaFlow Liberty® for Severe BAV StenosisEnrolling by invitationNCT06597188Not applicable
- VitaFlow LIBERTY EuropeRecruitingNCT06535659
- Registration Trial of the Intracranial Visualized Stent for the Wide-necked Intracranial Aneurysms:REBRIDGERecruitingNCT06189950Not applicable
- A PROSPECTIVE, MULTICENTER, SINGLE-ARM TRIAL FOR THE NEW SIZES OF BRIDGE STENTS FOR VERTEBRAL ARTERY STENOSIS: Bridge-MAXRecruitingNCT06186024Not applicable
- EVOLUTION® Revision STEMMED CS Post Market Clinical Follow-up Study ProtocolRecruitingNCT06142669
- VitaFlow® Transcatheter Aortic Valve Replacement System Pre-market Trial Long Term Follow Up （VITAL）Not yet recruitingNCT05977257
- A Trial of DCB vs DES in the Treatment of de Novo Large Diameter Coronary Atherosclerotic Stenosis(LARGE ONE)RecruitingNCT05961787Not applicable
- PARAT PLUS (The Tubridge Plus For The Treatment Of Wide-Necked Intracranial Aneurysms)RecruitingNCT05898893Not applicable
- CRATOS - Evaluation of Cratos™ Branch Stent Graft System in Treatment of Descending Aorta LesionsRecruitingNCT05874206Not applicable
- Post-market Surveillance of Micorport CRM Cardiac Implantable Electronic DevicesRecruitingNCT05694572
- Coronary Covered Stents Implantation for the Treatment of Coronary Artery PerforationRecruitingNCT05398991Not applicable
- Clinical Assessment of Essential Remote Monitoring Functions in PacemakersRecruitingNCT05165095
- Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing InsertEnrolling by invitationNCT04816773
- VitaFlow™ II Transcatheter Aortic Valve System Pre-market TrialRecruitingNCT04414878Not applicable
- VitaFlow™ Transcatheter Aortic Valve System Post-market Study-The LAUNCH StudyRecruitingNCT04414865
- Trial for MicroPort's DCBNot yet recruitingNCT04386213Not applicable
- Post Market Clinical Follow-Up Study for PROFEMUR® Preserve Classic Femoral StemEnrolling by invitationNCT04147559
- Post Market Clinical Follow-Up Study- EVOLUTION® Revision CCKEnrolling by invitationNCT04145401
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Z Revision Femoral StemsEnrolling by invitationNCT04064008
- Post Market Clinical Follow-Up Study Protocol for PROCOTYL® C Acetabular ComponentsEnrolling by invitationNCT03576573
- OCT vs IVUS vs QCA to Guide Moderate-to-severe Calcified Lesion Stent ImplantationRecruitingNCT03574636Not applicable
- Evaluation of New Specifications (2.25mm) of FirehawkTM in the Treatment of Coronary Heart Disease ( Firehawk_2.25 )CompletedNCT02688868Not applicableResults posted
- Evaluation of New Specifications (38mm) of FirehawkTM in the Treatment of Coronary Heart DiseaseCompletedNCT02688842Not applicableResults posted
- The First-In-Man Pilot Study of FirehawkCompletedNCT02688829Not applicableResults posted
- Observational Registry Study: FIREHAWK DES for Treating Coronary Artery Disease (CAD)CompletedNCT01412164Not applicableResults posted
- Inappropriate Shock Reduction wIth PARAD+ Rhythm DiScriminationCompletedNCT01410552Not applicableResults posted
- Randomized MicroPort's Firehawk DES Versus Xience V: TARGET I TrialCompletedNCT01196819Not applicableResults posted
- Ceramic on Metal Total Hip Replacement System Multi-Center,Investigational Device Exemption Clinical TrialTerminatedNCT00820443Phase 4Results posted
- Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing InsertActive, not recruitingNCT07391592
- Alwide Plus China Post-market Clinical InvestigationCompletedNCT07304427
- Intracranial Distal Access Catheter in Neurointerventional TherapyCompletedNCT06989931
- Bioabsorbable/Nufairy Coil Application Trial in ChinaActive, not recruitingNCT06466564Not applicable
- Safety and Performance Evaluation of a New Catheter Range for Lead Implantation at Interventricular SeptumCompletedNCT06453850Not applicable
- A Dual Energy Catheter (PFA and RFA) and a PFA Catheter for the Treatment of PeAFCompletedNCT06232798Not applicable
- PROSPECTIVE, MULTI-CENTER, OPEN-LABEL, SINGLE-ARM REGISTRATION TRIAL OF THE TUBRIDGE FOR THE TREATMENT OF WIDE-NECKED SMALL AND MEDIUM-SIZED INTRACRANIAL ANEURYSMSStatus unknownNCT05829746Not applicable
- A Multicenter Study of Pulsed Field Ablation for Paroxysmal Supraventricular TachycardiaCompletedNCT05820035Not applicable
- Coronary Intravascular Lithotripsy System in Patients With Coronary Artery Calcification (VIGOUR)CompletedNCT05818098Not applicable
- Coronary Crossing System in Patients With Coronary Chronic Total OcclusionsCompletedNCT05813704Not applicable
- Tubridge Flow Diverter Study For Intracranial AneurysmsStatus unknownNCT05646108
- Coronary Non-slip Balloon Catheter in Patients With Coronary Artery Stenosis(CREST)Status unknownNCT05606367Not applicable
- Coronary Atherectomy System in Patients With Coronary Calcification (CORECT)CompletedNCT05447585Not applicable
- PoSt-market Assessment on Safety and Performance of J-sHAPed xFINE LeadStatus unknownNCT05440071
- Registration Trial of the Intracranial Visualized Stent for the Wide-necked Intracranial AneurysmsStatus unknownNCT05275296Not applicable
- Collection of SPOT EGMs And inTra-Cardiac Impedance for Atrio-ventricUlar and inteR-ventricular Delays optimizatioNStatus unknownNCT05019833Not applicable
- TARGET-PREMIER Trail in Evaluating the Safety and Efficacy of the Rapamycin Target Eluting Stent in CAS TreatmentActive, not recruitingNCT04951050Not applicable
- Compare Sirolimus Coated Balloon Catheter With Paclitaxel Coated Balloon Catheter in De Novo Coronary Bifurcated LesionsActive, not recruitingNCT04918615Not applicable
- Evaluation of a Modified Anti-Platelet Therapy Associated With Low-dose DES Firehawk in Acute Myocardial Infarction Patients Treated With Complete Revascularization StrategyCompletedNCT04753749Not applicable
- VitaFlow™ Transcatheter Aortic Valve System Pre-market TrialStatus unknownNCT04655742Not applicable
- Post Market Clinical Follow-Up Study for MicroPort PROFEMUR® Preserve Classic Femoral StemWithdrawnNCT04615039
- Safety and Performance of INVICTA Ventricular DF4 LEADS With Active Fixation-(APOLLO)CompletedNCT04590144Not applicable
- Firehawk Rapamycin Target Eluting Coronary Stent North American TrialActive, not recruitingNCT04562532Not applicable
- Safety and Efficacy of Rotator Cuff Function Restoration Balloon in Irreparable Rotator Cuff TearStatus unknownNCT04538001Not applicable
- Using Left Atrium Appendage Closure in NVAF Patients With High Risk of Ischemic StrokeActive, not recruitingNCT04479722Not applicable
- Assessment of the Axone Micro Quadripolar Lead for Enhanced Cardiac Resynchronization TherapyActive, not recruitingNCT04463641Not applicable
- Post Market Clinical Follow-Up Study for EVOLUTION® BIOFOAM® Tibia and EVOLUTION® CS/CR Porous FemurActive, not recruitingNCT04301622
- Observational Study on Inappropriate TherapiesActive, not recruitingNCT04118803
- Safety and Electrical Performances of XFINE LeadsCompletedNCT03922386Not applicable
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Preserve Femoral StemActive, not recruitingNCT03865667
- Clinical Investigation of ENO/TEO/OTO Pacing System Under MRI EnvironmentStatus unknownNCT03811691Phase 4
- Safety and Electrical Performance Evaluation of INVICTA Leads Models Equipped With DF4 ConnectorStatus unknownNCT03766919Not applicable
- Trial for MicroPort's Firesorb BVS: FUTURE-IIIStatus unknownNCT03660202Not applicable
- VitaFlowTM II Transcatheter Aortic Valve System StudyStatus unknownNCT03575039Not applicable
- Wright Medical Technology Metal-on-Metal 522 Post-Market Surveillance StudyCompletedNCT03450733
- Comparison One vs Six Months of Dual Antiplatelet Therapy After Implanted Firehawk TM Stent in High Bleeding Risk Patients With Coronary Artery DiseaseStatus unknownNCT03287167Phase 4
- Safety and Electrical Performances Evaluation of Navigo Leads Equipped With IS4 ConnectorStatus unknownNCT03279484Not applicable
- Firehawk™ Coronary Stent System in the Treatment of Coronary Chronic Total Occlusion Lesion(s)Status unknownNCT03040934Not applicable
- Comparison Three vs Twelve Months of Dual Anti-Platelet Therapy After Stent ImplantationStatus unknownNCT03008083Phase 4
- CATCH [Short Name for: Coil Application Trial in China]CompletedNCT02990156Not applicable
- Aorfix Intelliflex First in Human StudyStatus unknownNCT02907762
- A Trial of Firesorb in Patients With Coronary Artery Disease: FUTURE-IICompletedNCT02890160Not applicable
- Evaluation of Bone Mineral Density Changes After Total Hip Replacement: A Two-Year Clinical and DXA AnalysisCompletedNCT02865447
- PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular ComponentsActive, not recruitingNCT02823834
- Radiostereometric Analysis (RSA) of the PROFEMUR® Preserve Classic Femoral ComponentsWithdrawnNCT02668211Not applicable
- A First-in-Man Study of the Firesorb BVS (FUTURE-I)CompletedNCT02659254Not applicable
- Gait and Functional Outcomes Study Following Total Knee Arthroplasty With Medial-pivot or Posterior-stabilized ImplantsCompletedNCT02589197
- Non-inferiority Study Comparing Firehawk Stent With Abbott Xience Family Stent (TARGET-AC)CompletedNCT02520180Not applicable
- PMCF Study for PROFEMUR® Am Femoral Components and PROCOTYL® O HA Coated Acetabular ComponentsWithdrawnNCT02507258
- AAA Registry: Clinical Outcomes of Highly Angulated anatomY Treated With the Aorfix™ Stent GraftSuspendedNCT02480595
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator Cemented Femoral StemsTerminatedNCT02397746
- Continued Access Clinical Trial of the SonRtip Lead and Automatic AV-VV Optimization Algorithm in the PARADYM RF SonR CRT-DStatus unknownNCT02374801Not applicable