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REVIVE-CVST Randomized Trial, Early EVT for Cerebral Venous Sinus Thrombosis, 440 Participants

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Summary

REVIVE-CVST is a multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE) trial evaluating whether early endovascular thrombectomy (EVT) combined with standard anticoagulation improves outcomes compared to anticoagulation alone in patients with severe cerebral venous sinus thrombosis (CVST). The trial aims to enroll 440 participants across approximately 15 centers in the Middle East, North Africa, South Asia, and Turkey (MENA-SINO network) over approximately 42 months, with primary endpoint assessment at 180 days via modified Rankin Scale shift analysis.

“REVIVE-CVST is a multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE) trial evaluating whether early endovascular thrombectomy (EVT) combined with standard anticoagulation improves outcomes compared to anticoagulation alone in patients with severe cerebral venous sinus thrombosis (CVST).”

NIH , verbatim from source
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ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

REVIVE-CVST is a newly registered clinical trial on ClinicalTrials.gov (NCT07548346) evaluating early endovascular thrombectomy (EVT) for severe cerebral venous sinus thrombosis. The trial will enroll 440 adult participants presenting within 14 days of symptom onset with imaging-confirmed CVST and at least one severity marker, randomized 1:1 to EVT plus anticoagulation versus anticoagulation alone. Primary endpoint is functional outcome at 180 days by modified Rankin Scale.

Healthcare facilities and clinical investigators, particularly those with stroke or neurointerventional capabilities in the MENA-SINO network regions, should be aware of this trial for potential participation or referral. The protocol is now publicly registered and may inform future clinical practice standards for severe CVST management.

Archived snapshot

Apr 23, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

MENA Regional Endovascular Intervention for Venous Cerebral Venous Sinus Thrombosis

N/A NCT07548346 Kind: NA Apr 23, 2026

Abstract

REVIVE-CVST is a multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE) trial evaluating whether early endovascular thrombectomy (EVT) combined with standard anticoagulation improves outcomes compared to anticoagulation alone in patients with severe cerebral venous sinus thrombosis (CVST).

The study targets adult patients (aged 18 years or older) presenting within 14 days of symptom onset with imaging-confirmed CVST and at least one severity marker, such as a Glasgow Coma Scale score of 14 or below, intracerebral hemorrhage, venous infarction, or deep venous system involvement.

Participants will be randomly assigned in a 1:1 ratio to either the intervention arm (EVT plus anticoagulation) or the control arm (anticoagulation alone). The primary endpoint is functional outcome at 180 days as measured by the modified Rankin Scale (mRS), using a shift analysis across all mRS categories.

The trial aims to enroll 440 participants across approximately 15 centers in the Middle East, North Africa, South Asia, and Turkey (MENA-SINO network). The study duration is approximately 42 months, including 18 months of enrollment and 12 months of follow-up for the last enrolled patient.

Conditions: Cerebral Venous Sinus Thrombosis

Interventions: Endovascular Thrombectomy, Anticoagulation Therapy

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Last updated

Classification

Agency
NIH
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Clinical investigators Healthcare providers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Clinical trial recruitment Medical device research Drug therapy evaluation
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Pharmaceuticals Medical Devices

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