Lifetech KONAR MFO Post-Market Clinical Follow-Up Study

Status Completed

Clinical Trial Summary

The purpose of the study is to collect real-world data on patient outcomes and evaluate the procedural success and performance of the Lifetech KONAR-MF™ VSD Occluder for patients with ventricular septal defect (VSD).

Clinical Trial Description

This is a non-randomized prospective post-marketing clinical follow-up study (PMCFS) in order to evaluate the feasibility and safety of the Lifetech KONAR-MF™ VSD Occluder device used for patients with ventricular septal defect. The implantation should be performed in accordance with the instructions for use (IFU). ;

Study Design

Related Conditions & MeSH terms

Heart Septal Defects, Ventricular
Ventricular Septal Defect

Clinical Trial Details

NCT number	NCT04417712
Study type	Observational
Source	Lifetech Scientific (Shenzhen) Co., Ltd.
Contact
Status	Completed
Phase
Start date	December 4, 2019
Completion date	June 30, 2023

View Details

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