SaExten Vena Cava Filter System in Prevention of Pulmonary Embolism

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of SaExten vena cava filter (VCF) system (ShenZhen KYD BioTech Co., Ltd., China) in prevention of pulmonary embolism (PE). This is a prospective, multicenter, randomized controlled, positive-controlled clinical trial, which will enroll 204 participants in total. Participants will undergo interventions with SaExten VCF System or Denali filter (C. R. BARD, Inc., USA).

Clinical Trial Description

The purpose of this study is to evaluate the efficacy and safety of SaExten vena cava filter (VCF) system in prevention of pulmonary embolism (PE). This is a prospective, multicenter, randomized controlled, positive-controlled clinical trial, which will enroll 204 participants in total, with 102 in each group. Participants will undergo interventions with SaExten VCF System or Denali filter, and be followed up to 12 months if the implantation is permanent, to evaluate the efficacy and safety of SaExten VCF System in prevention of PE. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04948502
Study type	Interventional
Source	ShenZhen KYD Biomedical Technology Co., Ltd.
Contact
Status	Completed
Phase	N/A
Start date	August 13, 2020
Completion date	September 8, 2022

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