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Study identifier: NCT06241677 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intravenous Thrombolytic Therapy in Acute Ischemic Stroke Patients on DOAC

Condition: CVA (Cerebrovascular Accident)  ·  Sponsor: Chinese University of Hong Kong

PhaseNA
Planned participants260
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Direct oral anticoagulants (DOAC) have emerged as safe and efficacious ischemic stroke prophylaxis for non-valvular atrial fibrillation (NVAF). All four DOACs - apixaban, dabigatran, edoxaban, rivaroxaban - were associated with lower risks of major bleeding compared to warfarin. Listed as core essential medicines by the World Health Organization, DOAC prescriptions have been surging worldwide. In Hong Kong, approximately 80,000 patients received DOACs from January 2009 through December 2022 according to the Hospital Authority registry. The widespread DOAC usage had created DOAC-specific clinical dilemmas that lack evidence-based treatment despite twenty years of prescribing experience. Ischemic stroke despite DOAC (IS-DOAC), in particular, may occur in up to 6% of DOAC users annually. Due to the in vivo anticoagulation effect, there had been concerns of intracerebral bleeding (ICH) with intravenous thrombolytic therapy (IVT) for acute IS-DOAC. Under the current guideline recommendations, most acute IS-DOAC are contraindicated to IVT (see Intravenous thrombolytic therapy), which resulted in only a small proportion of acute ISDOAC patients being able to receive IVT even if presented early. Nonetheless, our group found that majority of patients had a DOAC level of \<50ng/mL only 24 hours after DOAC cessation (see work done by us), a level deemed clinically negligible and safe for thrombolytic therapy. Together with evolving clinical evidence discussed below, IS-DOAC patients ma…

This description comes directly from the study's public registry record.

Talk to the study team

Yiu Ming Bonaventure Ip, MB ChB  ·  +852-26352152  ·  bonaventureip@cuhk.edu.hk

Trista Hung  ·  +852-26352152  ·  tristahung@cuhk.edu.hk

Always discuss trial participation with your own doctor first.

Locations (1)

Chinese University of Hong KongHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT06241677