Neurovascular Nuggets_ Rivaroxaban for Cerebral Venous Thrombosis – Unpacking a Feasibility Trial
Study of Rivaroxaban for Cerebral Venous Thrombosis: A Randomized Controlled Feasibility Trial Comparing Anticoagulation With Rivaroxaban to Standard-of-Care in Symptomatic Cerebral Venous Thrombosis Here are the key points from the research article on rivaroxaban vs standard-of-care for cerebral venous thrombosis (CVT): - The study was a randomized controlled feasibility trial conducted at 12 Canadian centers comparing rivaroxaban to standard anticoagulation (warfarin or low molecular weight heparin) for CVT. - 55 participants were enrolled over 2.5 years. The recruitment rate was 21.3 participants per year, meeting feasibility targets. 57% of eligible patients consented to enroll. - Median age was 48 years and 66% were female. Median time from diagnosis to enrollment was 3 days. - One patient on rivaroxaban had a symptomatic intracranial hemorrhage by day 180 (primary safety outcome), compared to none in the control group. Rates of clinically relevant non-major bleeding and recurrent CVT were also numerically higher with rivaroxaban. - All patients had at least partial recanalization by day 180 on imaging. - Despite over 75% having functional independence at baseline per mRS scores, participants reported impairments in quality of life, mood, fatigue, headaches and cognition at enrollment. All patient-reported metrics improved by days 180 and 365. - The authors conclude that recruitment targets were met but consent rates were suboptimal. Early safety signals potentially favor standard anticoagulation but overall event rates were low. Patient-reported outcomes suggest CVT impacts well-being despite mild stroke severity. Larger trials are needed to confirm safety and optimize antithrombotic therapy. Read more at https://lnkd.in/d6aEiydK