Atrial Fibrillation Trial, Recruiting NCT05378035 Sponsor: Chinese University of Hong Kong Condition: Atrial Fibrillation
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Atrial Fibrillation Trial, Recruiting

NCT05378035
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People of Chinese background who have a type of irregular heartbeat (called non-valvular atrial fibrillation) and have been taking one of these blood-thinning medicines for 6 months or more: apixaban, dabigatran, edoxaban, or rivaroxaban.
  • People between 18 and 80 years old.
  • People who are able to give their written agreement to take part in the trial.
  • People who are already scheduled for a planned medical procedure that requires their blood-thinning medicine to be paused for 48 hours.

Who may not be able to join:

  • People who had a blood clot (such as a stroke or bowel blockage from a clot) or a serious bleeding event (such as bleeding in the brain or stomach) while taking their blood-thinning medicine.
  • People whose kidneys are not filtering blood well enough, based on a specific medical measurement (confirm with trial site).
  • People who are taking a dose of their blood-thinning medicine that does not match what is recommended for their age, weight, and kidney function.
  • People who are taking their blood-thinning medicine for a reason other than non-valvular atrial fibrillation, such as a history of a narrowed heart valve, a mechanical heart valve, a clotting disorder, or blood clots in the veins or lungs.
  • People who have other health conditions that affect how their blood clots, beyond the use of their blood-thinning medicine — such as certain blood cell disorders, liver congestion, or liver failure affecting clotting.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 19 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Bonaventure Yiu Ming IP, MB ChB, Chinese University of Hong Kong

Phone: 852-28902002

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
28 September 2022
Est. completion
27 September 2027

Where this trial is recruiting

Hong Kong

Primary endpoints

Specific coagulation assays; Liquid chromatography-mass spectrometry; Pharmacogenomics

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov