A Multicenter, International, Follow-up Study to Monitor the Efficacy and Safety of the Occlutech® PmVSD Occluder in Patients With Perimembranous Ventricular Septal Defects

Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membranous VSD OCCLUDER

NCT00578708 ·Status: COMPLETED ·Phase: PHASE1

Implantation of a Permanent Interatrial Shunt to Reduce Left Atrial Filling Pressures Following MitraClip

NCT04729933 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA

MitraClip® and Hemodynamic Effects of Relevant Iatrogenic Atrial Septum Defect Closure

NCT03024268 ·Status: UNKNOWN ·Phase: NA

Procedural Success and Safety of the Nit-Occlud® Patent Foramen Ovale (PFO) Closure Device and Its Application System

NCT00968032 ·Status: COMPLETED ·Phase: NA

Study on the Safety and Effectiveness of the SnowyTM PFO Closure System

NCT05360771 ·Status: NOT_YET_RECRUITING ·Phase: NA

Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD Occluder

NCT00583791 ·Status: COMPLETED ·Phase: NA

Lifetech KONAR MFO Post-Market Clinical Follow-Up Study

NCT04417712 ·Status: COMPLETED

Safety and Effectiveness of the Nit-Occlud® Lê VSD Spiral Coil System

NCT00390702 ·Status: COMPLETED ·Phase: NA

Safety and Efficacy of the GORE® Septal Occluder to Treat Ostium Secundum Atrial Septal Defects

NCT01711983 ·Status: COMPLETED ·Phase: NA

Early Feasibility EXperience of Posterior Leaflet RestOration to REduce Mitral Regurgitation

NCT04098328 ·Status: TERMINATED

Evaluation of the GORE PV1 Device in Patients With Pulmonary Valve Dysfunction

NCT03441971 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA

Phase II Clinical Trial of Percutaneous Ventricular Restoration Using Heartech® Device Preventing Heart Failure Post Myocardial Infarction (The Partical Study)

NCT04039256 ·Status: UNKNOWN ·Phase: NA

Safety Study of Octreotide Injection to Prevent GI Bleeding in Patients With Left Ventricular Assist Device (LVAD)

NCT01707225 ·Status: COMPLETED ·Phase: PHASE1

Veno-arterial Extracorporeal Membrane Oxygenation Prior to Left Ventricular Assist Device Implantation.

NCT03583970 ·Status: UNKNOWN

Safety and Efficacy Study of the BioVentrix PliCath HF System

NCT01568164 ·Status: COMPLETED ·Phase: NA

The V-Wave Shunt: FIM Safety and Feasibility Study

NCT01965015 ·Status: COMPLETED ·Phase: NA

Magenta Elevate™ Clinical Feasibility Study in Cardiogenic Shock

NCT07293923 ·Status: RECRUITING ·Phase: NA

Efficacy and Safety of the CorVad Percutaneous Ventricular Assist System in Cardiogenic Shock

NCT06646224 ·Status: RECRUITING ·Phase: NA

To Evaluate the Efficacy and Safety of the Transfemoral Mitral Valve Repair System in the Treatment of Patients With Moderately Severe and Severe Functional Mitral Regurgitation(FMR) Who Remained Clinically Symptomatic After Guideline-directed Medical Treatment

NCT05508438 ·Status: NOT_YET_RECRUITING ·Phase: NA

Long-term Safety Study of the GORE® HELEX® Septal Occluder

NCT00581308 ·Status: COMPLETED ·Phase: NA

Outcomes of a Novel Magnetically Levitated LVAD: a Multicenter Analysis

NCT06596499 ·Status: COMPLETED

Rivet PVS Therapy in Group 2 PH-HFpEF Canada

NCT05332873 ·Status: WITHDRAWN ·Phase: NA

Aachen Safety and Efficacy of the Percutaneous Transvenous Mitral Annuloplasty Device to Reduce Mitral Regurgitation

NCT00572091 ·Status: COMPLETED ·Phase: PHASE1/PHASE2

Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investigational Device Exemption Cohort

NCT00740870 ·Status: COMPLETED ·Phase: NA

Mi-STITCH™ and Mi-KNOT™ Device Technologies - Improvement of Mitral Valve Repair

NCT05034471 ·Status: UNKNOWN ·Phase: NA