Safety and Effectiveness Study of the Solysafe Septal Occluder
NCT00353509 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL
Last updated 2013-10-09
Summary
Prospective mono-center clinical study to evaluate the safety and effectiveness of an intracardiac septal closure device in patients with atrial septum defect (ASD)
Conditions
- Atrial Septal Defects
Interventions
- DEVICE
-
Device Closure of a Septal Defect
Sponsors & Collaborators
-
Carag AG
lead INDUSTRY
Principal Investigators
-
Ida Jovanovic, Prof. Dr. · University Children's Hospital Belgrade
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 2 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- Serbia
Study Locations
More Related Trials
-
Safety and Efficacy Study of Absnow Absorbable ASD Closure System For Treating ASD Patients
NCT03601039 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
NCT01531374 ·Status: COMPLETED ·Phase: NA
-
Cera™ ASD Occluder Post-Market Clinical Follow-Up Study
NCT06849635 ·Status: RECRUITING
-
Platelet Adhesion in the Pathobiology of Aortic Stenosis
NCT05550896 ·Status: ACTIVE_NOT_RECRUITING
-
SecOnd-generation seLf-expandable Versus Balloon-expandable Valves and gEneral Versus Local Anesthesia in TAVI
NCT02737150 ·Status: UNKNOWN ·Phase: NA
-
Valvosoft First-In-Human Study in Severe Symptomatic Aortic Stenosis
NCT04665596 ·Status: COMPLETED ·Phase: NA
-
Stitch Closure of PFO and Septal Repair
NCT03373929 ·Status: UNKNOWN ·Phase: NA
-
CryoValve SG Pulmonary Human Heart Valve Post Clearance Study
NCT01092442 ·Status: COMPLETED
-
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 Replacement
NCT01675440 ·Status: COMPLETED
-
Outcomes of Transcatheter Aortic Valve Implantation in Management of Severe Symptomatic Aortic Stenosis
NCT03633383 ·Status: UNKNOWN
-
Assessment of Arrhythmias in Patients Undergoing Transcatheter Aortic Valve Implantation Using a Small Insertable Cardiac Monitoring Device
NCT02559011 ·Status: COMPLETED
-
Early Feasibility Study for the Foldax Tria Aortic Heart Valve
NCT03851068 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Myval Global Study of Myval™ THV Series Implanted in Patients With Native Severe Aortic Valve Stenosis.
NCT04703699 ·Status: RECRUITING
-
Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Transcatheter Aortic Valve Implantation
NCT02504632 ·Status: COMPLETED ·Phase: NA
-
Electrocardiographic and Electrophysiologic Changes After Percutaneous Closure of Atrial Septal Defect
NCT06761807 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Treatment of Severe Secondary TRIcuspid Regurgitation in Patients With Advance Heart Failure With CAval Vein Implantation of the Edwards Sapien XT VALve (TRICAVAL)
NCT02387697 ·Status: TERMINATED ·Phase: PHASE2/PHASE3
-
Colchicine for Patients With Aortic Stenosis Undergoing Transcatheter Aortic Valve Replacement
NCT04870424 ·Status: COMPLETED ·Phase: PHASE3
-
A Clinical Evaluation of the HYDRA Self Expanding Transcatheter Aortic Valve
NCT02434263 ·Status: UNKNOWN ·Phase: NA
-
CoreValve™ Evolut R™ FORWARD Study
NCT02592369 ·Status: COMPLETED
-
CoreValve Advance International Post Market Study
NCT01074658 ·Status: COMPLETED
-
Efficacy of Three Dimensional Transesophageal Echocardiography for Percutaneous Device Closure in Atrial Septal Defect
NCT02097758 ·Status: RECRUITING ·Phase: NA
-
Aortic Valve replAcement in eLective Patients From aOrtic Valve multiceNter Registry
NCT05308173 ·Status: COMPLETED
-
Transcatheter Closure Versus Surgery of Perimembranous Ventricular Septal Defects
NCT00890799 ·Status: COMPLETED ·Phase: NA
-
The ShortCut™ Study Protocol
NCT04952909 ·Status: COMPLETED ·Phase: NA
-
A Multicenter, International, Prospective and Retrospective, Follow-up Registry to Monitor the Efficacy and Safety of the Occlutech Paravalvular Leak Device (PLD) in Patients With Mitral or Aortic Paravalvular Leaks
NCT07037446 ·Status: ENROLLING_BY_INVITATION