Clinical Trial

Levetiracetam for Seizure Prevention After Brain Tumor Surgery

Study acronym: PREVENT
Recruiting Phase 3
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Summary
This study aims to evaluate the efficacy and safety of levetiracetam for the prevention of postoperative seizures in adult patients undergoing supratentorial brain tumor surgery. It is a multicenter, randomized, double-blind, placebo-controlled, parallel-group clinical trial. Eligible participants will be randomly assigned in a 1:1 ratio to receive levetiracetam or placebo, starting 1 hour before surgery and continuing for 3 months postoperatively. The primary outcome is the incidence of clinical seizures within 3 months after surgery. Secondary outcomes include subclinical seizures within 7 days and 3 months postoperatively, adverse events within 3 months, and health economic outcomes. The study aims to clarify the role of levetiracetam in the primary prevention of perioperative seizures in brain tumor patients and to provide evidence for rational use of antiseizure medications in neurosurgical practice.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-11-16.
Status change: Not Yet Recruiting → Recruiting 2026-05-26
Trial Details
NCT Number NCT07239115
Lead Sponsor Beijing Tiantan Hospital
Conditions Postoperative Seizures After Brain Tumor Surgery
Enrollment 558 participants
Start Date 2026-05-14
Primary Completion 2027-01 (estimated)
Study Completion 2027-06 (estimated)
Updated on ClinicalTrials.gov 2026-05-28