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Clinical Trial Summary

The purpose of this study is to explore the efficacy, safety and cost-effectiveness of Xueshuantong (lyophilized) for the prevention of venous thromboembolism (VTE) in patients at risk of bleeding.


Clinical Trial Description

This is a non-randomized, observational study. This study primarily aims to investigate the efficacy, safety, and cost-effectiveness of using Xueshuantong injection (lyophilized) for preventing venous thromboembolism (VTE) in patients susceptible to bleeding. The subjects of the study comprise patients during the perioperative period (undergoing procedures lasting 45 minutes or longer), patients with a confirmed spontaneous cerebral hemorrhage (ICH), and patients with a confirmed acute ischemic stroke (AIS). Additional objectives of this study including: 1. to evaluate the possible dose-dependency of Xueshuantong injection (lyophilized); 2. to evaluate the impact in coagulation function after administration of Xueshuantong injection (lyophilized) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06443905
Study type Observational
Source China-Japan Friendship Hospital
Contact
Status Active, not recruiting
Phase
Start date August 1, 2023
Completion date December 30, 2024

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