Intravenous Thrombolytic Therapy in Acute Ischemic Stroke Patients on DOAC

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorChinese University of Hong Kong

About this trial

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 maybe unnecessarily barred from IVT, thus compromised functional recovery.

With robust pharmacokinetic and retrospective clinical evidence to support, it is hypothesized that IVT are safe in IS-DOAC patient. The investigators hereby propose a prospective multicenter study to determine the efficacy and safety of IVT in acute IS-DOAC.

Eligibility criteria

Qualifiers

Acute ischemic stroke patients with a last-known-well to presentation time within 4.5 hours

Patients who took any doses of apixaban (2.5mg or 5mg twice daily), dabigatran (110mg or 150mg twice daily), edoxaban (30mg or 60mg daily) or rivaroxaban (15mg or 20mg daily) 12-48 hours before presentation

National Institute of Health Stroke Scale (NIHSS) ≥ 3

Alberta Stroke Programme Early CT (ASPECT) score ≥ 6

Disqualifiers

Initial CT brain showing intracranial haemorrhage

Contraindications to IVT according to current guideline recommendations [5], except for the use of DOAC within 12-48 hours

Patients with an estimated glomerular filtration rate of ≤ 30ml/min/1.73m2

Patients with bleeding propensities apart from the use of DOAC, e.g. platelet count of < 100x109/L

Trial design

Treatments tested in this trial

  • alteplase or tenecteplase

Treatment groups

260 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Chinese University of Hong Kong

Lead sponsor

Pamela Youde Nethersole Eastern Hospital

Collaborator

Queen Mary Hospital, Hong Kong

Collaborator

Princess Margaret Hospital, Canada

Collaborator

Tuen Mun Hospital

Collaborator

The Queen Elizabeth Hospital

Collaborator

United Christian Hospital

Collaborator