The SIFT trial is a pragmatic phase III, multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE), registry-linked trial. It is designed to test the hypothesis that intravenous thrombolysis (IVT) is both safe and effective in patients with acute ischemic stroke (AIS) who have ingested a Factor Xa (FXa) inhibitor within the last 48 hours and are otherwise eligible for IVT. The study aims to address the current limitations in stroke guidelines, which recommend against IVT in these patients due to concerns of symptomatic intracranial hemorrhage (sICH). However, these recommendations are based on data from vitamin K antagonist (VKA) studies rather than direct evidence from randomized clinical trials (RCTs) involving FXa inhibitors. Observational data suggest that IVT in patients on FXa inhibitors is safe and effective, but a well-monitored RCT is necessary to confirm these findings.
All treatment and monitoring routines in the study follow hospital standard operating procedures (SOPs), and both alteplase (ALP) and tenecteplase (TNK) are approved drugs for AIS, with similar efficacy and safety profiles. IVT is known to be an effective treatment for disabling AIS, improving functional outcomes when administered within 4.5 hours of symptom onset. FXa inhibitors have largely replaced warfarin due to their better safety profile, reducing the risk of hemorrhagic complications by 50% compared to VKAs. The concern over sICH remains a major reason why patients on FXa inhibitors are often excluded from IVT, yet research suggests that the net benefit of IVT outweighs the risks, even with an sICH rate of up to 8%.
The primary objective of the study is to compare early neurological improvement (ENI) in patients treated with IVT versus those receiving standard care. Secondary objectives include assessing clinical neurological improvement, infarct volume changes on imaging, functional outcomes, rates of sICH, any intracranial hemorrhage (ICH) after IVT, and overall mortality. The study has a planned recruitment of 300 patients, with a 2:1 allocation favoring IVT. The sample size is designed to provide sufficient power for primary and secondary analyses, including the safety assessment of sICH rates. The study will be conducted across emergency departments and acute stroke units in Norway.
Eligibility criteria include patients aged 18 or older who have ingested an FXa inhibitor within 48 hours before symptom onset (or have an ongoing prescription if the exact timing of last ingestion is unknown). Patients must have a clinical diagnosis of AIS with disabling neurological deficits and present within 4.5 hours of symptom onset or after awakening with symptoms, confirmed by imaging. Informed consent is required. Patients with contraindications to alteplase or tenecteplase, those planned for endovascular treatment due to isolated large vessel occlusion (LVO) in the internal carotid artery (ICA) or middle cerebral artery (MCA) with expected rapid intervention, those using dabigatran, or those deemed at high risk by their treating physician are excluded.
Participants randomized to the IVT arm will receive either alteplase (0.9 mg/kg with a 10% bolus and 90% infusion over 60 minutes) or tenecteplase (0.25 mg/kg single bolus) according to local SOPs. The control group will receive 300 mg of aspirin and no IVT, in line with current practice guidelines. The study duration is planned from 2025 to 2029, with termination by December 2030 unless safety concerns necessitate earlier closure. The estimated duration of patient follow-up is 90 days.
The study follows an open-label, blinded-endpoint design, with patient randomization handled via a computerized system (Viedoc). Randomization is stratified by age and baseline NIH Stroke Scale (NIHSS) score. The primary outcome measure is early neurological improvement, defined as an NIHSS reduction of ≥8 points or an NIHSS score of 0-1 at 24 hours. Secondary outcomes include percentage change in NIHSS from baseline, infarct volume at 24 hours, functional outcomes at 90 days, and the incidence of sICH and any ICH within 36 hours. Death within 90 days is also assessed.
The primary analysis will use a logistic regression model, adjusting for age, NIHSS score, and time to treatment. Safety monitoring will be continuous, with an early stopping mechanism in place if the sICH rate in the IVT arm is deemed unacceptably high. The study's impact could be substantial; if IVT is proven safe and effective in AIS patients on FXa inhibitors, it would significantly influence stroke management, enabling more patients to receive IVT and reducing post-stroke disability. These findings would contribute to international discussions and could lead to guideline changes worldwide, allowing all IVT-capable centers to offer immediate, effective treatment to a growing patient population.
