drugset / Trial / NCT00394901

A 13-Week, Randomized, Double-Blind, Multicenter, Placebo-Controlled Study Of Pregabalin For Postherpetic Neuralgia

NCT00394901 ↗

Phase 3 Completed 372 enrolled Viatris Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate efficacy and safety of pregabalin in the treatment of postherpetic neuralgia in a dose-ranging manner.

Timeline

Start
2006-09
Primary completion
2007-11
Completion
2007-11

Outcome

Mixed primary results

registry analysis (unspecified test); Placebo vs Pregabalin 150 mg/Day; p = 0.262; Mean Difference (Final Values) -0.31 (95% CI -0.85 to 0.23); ANCOVA NCT00394901 ↗

registry analysis (unspecified test); Placebo vs Pregabalin 300 mg/Day; p = 0.002; Mean Difference (Final Values) -0.86 (95% CI -1.39 to -0.32); ANCOVA NCT00394901 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Pregabalin Small molecule 150 mg Oral
Subject Pregabalin Small molecule 300 mg Oral
Subject Pregabalin Small molecule 600 mg Oral