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Efficacy and safety of RivaroXaban and DAbigatran versus AcenocouMarol in Cerebral Venous Thrombosis

Efficacy and safety of RivaroXaban and DAbigatran versus AcenocouMarol in Cerebral Venous Thrombosis (EXAMinCVT)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202202477162480
Enrollment
60
Registered
2022-02-10
Start date
2019-04-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nervous System Diseases

Interventions

Dabigatran
rivaroxaban

Sponsors

Hasan II University Hospital of Fez
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Informed consent written in accordance with the rules of good clinical practice and laws in force in the country. 2. Confirmed diagnosis of venous or cerebral thrombosis (DVT), with or without intracranial hemorrhage (CT scan injected or brain MRI) 3. Curative dose anticoagulant (LMWH) therapy that has been administered from confirmation of diagnosis to randomization; 4. Eligibility for oral anticoagulant therapy.

Exclusion criteria

Exclusion criteria: 1. Cerebral venous thrombosis (CVT) associated with central nervous system infection or head trauma. 2. Medical or surgical conditions associated with an increased risk of bleeding 3. History of symptomatic nontraumatic intracranial hemorrhage at high risk of recurrence 4. Treatment with an antithrombotic regimen for an indication other than CVT and requiring continuation of this treatment for the initial diagnosis without modification of the treatment regimen 5. Severe renal insufficiency 6. Active hepatopathy 7. Pregnancy ongoing or planned during the clinical trial 8. Any contraindications to VKA or NOAC.

Design outcomes

Primary

MeasureTime frame
Mortality (any cause) in the year following randomization, major bleeding or new venous thrombotic event (VTE)

Secondary

MeasureTime frame
Cerebral venous recanalization measured by change in the number of occluded cerebral veins and dural sinuses after 24 week. ;Number of patients with clinically significant non-major bleeding events after 24 weeks

Countries

Morocco

Contacts

Public ContactNaima Chtaou

Assistant Professor

naimachtaou@gmail.com+212664838010

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026