Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER

See also
Status	Clinical Trial	Phase
Terminated	`NCT00229827` - Optimal Timing for Repair of Left to Right Shunt Lesions	N/A
Completed	`NCT00890799` - Transcatheter Closure Versus Surgery of Perimembranous Ventricular Septal Defects	N/A
Completed	`NCT02552485` - Evaluation of Latent Pulmonary Arterial Hypertension in Congenital Shunt Lesions	N/A

See also

Status

Clinical Trial

Phase

Terminated

NCT00229827 - Optimal Timing for Repair of Left to Right Shunt Lesions

N/A

Completed

NCT00890799 - Transcatheter Closure Versus Surgery of Perimembranous Ventricular Septal Defects

N/A

Completed

NCT02552485 - Evaluation of Latent Pulmonary Arterial Hypertension in Congenital Shunt Lesions

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00647387
Study type	Interventional
Source	Abbott Medical Devices
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 2008
Completion date	August 2025

Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscular VSD (MuVSD) Occluder - Post Approval Study — VPA

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms