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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


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

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