drugset / Trial / NCT00071721

Valproate in Dementia (VALID)

NCT00071721 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to demonstrate whether valproate therapy delays the emergence of agitation and/or psychosis in outpatients with probable Alzheimer's disease (AD) who have not experienced agitation and psychosis in their illness. A secondary aim is to determine whether valproate therapy delays the progression of cognitive and functional measures of the illness. This trial will also assess the tolerability and safety of low-dose, long-term valproate therapy. Valproate, an anticonvulsant drug, was selected because of its possible symptomatic efficacy for agitation in AD, known safety profile in numerous clinical populations, and in view of recent data supporting its neuroprotective potential in AD.

Timeline

Start
2003-10
Primary completion
2009-02
Completion
2009-12

Outcome

Missed primary endpoint

paper There was no difference between groups in time to emergence of agitation or psychosis (Cox proportional hazard ratio, 0.96; P = .88). PMID 21810649 ↗

paper Valproate treatment did not delay emergence of agitation or psychosis PMID 21810649 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Valproate Small molecule 10 mg/kg —
Subject Valproate Small molecule 12 mg/kg —

Indications