Monitoring of NOAC Therapy: Standardizing Reference Intervals

NCT04611893 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 308

Last updated 2026-02-24

No results posted yet for this study

Summary

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

Conditions

Sponsors & Collaborators

  • Chinese University of Hong Kong

    lead OTHER

Principal Investigators

  • Yiu Ming Bonaventure IP, MRCP · Chinese University of Hong Kong

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-11-05
Primary Completion
2025-06-30
Completion
2025-06-30

Countries

  • Hong Kong

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04611893 on ClinicalTrials.gov