Viewing Study NCT04611893


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Study NCT ID: NCT04611893
Status: RECRUITING
Last Update Posted: 2024-12-06
First Post: 2020-10-27
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Monitoring of NOAC Therapy: Standardizing Reference Intervals
Sponsor: Chinese University of Hong Kong
Organization:

Study Overview

Official Title: Monitoring of NOAC Therapy: Standardizing Reference Intervals
Status: RECRUITING
Status Verified Date: 2024-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is aimed to establish reference intervals of NOAC (dabigatran, apixaban and rivaroxaban) in ethnic Chinese patients.
Detailed 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 Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: