Comparison of the Efficacy of Rivroxaban to Coumadin( Warfarin ) in Cerebral Venous Thrombosis (CVT)
Cerebral Venous Thrombosis
About this trial
This is an interventional health services research trial for Cerebral Venous Thrombosis
Eligibility Criteria
Inclusion Criteria:
Patients of either gender Age between 13 years and 50 years Patients with proven CVT on neuro imaging (CTV, o MRV) -
Exclusion Criteria:
Patients suffering from Chronic Liver disesase Patients having contraindications for oral anticoagulation Patients suffering from hematological or brain malignancy Patients whose MRV and CTV do not support CVT
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Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Coumadin Group
Rivoroxaban Group
Patients in Coumadin Group would be administered Coumadin with overlap of heparin for first two days followed by Coumadin given orally ,dose being adjusted according to INR .The INR range would be between 2-3.it would be given once a day.The total duration OFf coumadin would be six months.
The dose protocol would be similar to the one used in Deep Venous Thrombosis. 15 mg PO q12hr for 21 days with food, THEN 20 mg PO qDay for 6 months.