Dabigatran Versus Rivaroxaban in Cerebral Venous Thrombosis

Recruiting Phase 3 Interventional Study
Cerebral Venous Sinus Thrombosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
200 (estimated)
Sponsor
Kafrelsheikh University · Other
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About This Trial

Along with the current clinical trial, the efficacy and safety of a 150 mg Bid dabigatran administered within 24 hours of randomization after having first-ever cerebral venous thrombosis compared to 20 mg rivaroxaban were assessed through rate of recurrent VTE, mRS, rate of venous recanalization, HIT score, MoCA test, and central and peripheral hemorrhagic complications

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 1-Patients aged 18 and above 2-New diagnosis of symptomatic cerebral venous thrombosis as confirmed on CT/CT venogram or MRI/MR venogram 3-Ability to randomize within 14 days of neuroimaging-confirmed diagnosis 4-The treating clinician thinks that the patient is appropriate fo…
Contacts

mohamed G. Zeinhom, MD

2001009606828

mohamed_gomaa@med.kfs.edu.eg

CONTACT

sherihan R. ahmed, MD

2001113432342

sherihan_rezq@med.kfs.edu.eg

CONTACT