Clinical Trials Directory

Trials / Completed

CompletedNCT00160511

A 16 Week Study Evaluating Levetiracetam in the Treatment of Post Herpetic Neuralgia (PHN)

A Double-blind, Randomized, Placebo-controlled, Parallel-group, 16 Week, Multicenter Trial Evaluating the Efficacy and Safety of Levetiracetam 500 mg Tablets in Bid Administration (Daily Dose Ranging From 1000 mg to 3000 mg), in Adults (≥ 18 Years of Age) Suffering From Postherpetic Neuralgia

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
170 (planned)
Sponsor
UCB Pharma · Industry
Sex
All
Age
18 Years
Healthy volunteers

Summary

16 week trial assessing the efficacy, safety, and tolerability of levetiracetam compared with placebo in the treatment of postherpetic neuralgia.

Conditions

Interventions

TypeNameDescription
DRUGLevetiracetam

Timeline

Start date
2004-04-01
Primary completion
2005-08-01
Completion
2005-09-01
First posted
2005-09-12
Last updated
2013-11-26

Source: ClinicalTrials.gov record NCT00160511. Inclusion in this directory is not an endorsement.