Monitoring of NOAC Therapy: Standardizing Reference Intervals

Status Recruiting

Clinical Trial Summary

This study is aimed to establish reference intervals of NOAC (dabigatran, apixaban and rivaroxaban) in ethnic Chinese patients.

Clinical Trial Description

360 patients who are on dabigatran, apixaban and rivaroxaban based on the above inclusion and exclusion criteria will be recruited. After the informed consent, the patient will be needed for blood taking before and 2 hours after the medication (NOAC). The patient's demographic data and medical history will also be retreived from Central Medical Syetem too. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04611893
Study type	Observational
Source	Chinese University of Hong Kong
Contact	Yiu Ming Bonaventure IP, MRCP
Phone	852-35053856
Email	iym984@ha.org.hk
Status	Recruiting
Phase
Start date	November 5, 2020
Completion date	August 31, 2024

View Details

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