Clinical Trials Directory

Trials / Completed

CompletedNCT00335933

Safety and Efficacy of Gabapentin in Postherpetic Neuralgia

A Phase 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of Gabapentin Extended Release (G-ER) Tablets in the Treatment of Patients With Postherpetic Neuralgia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
378 (estimated)
Sponsor
Depomed · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Gabapentin and pregabalin are treatments for some types of neuropathic pain, including postherpetic neuralgia (PHN). However, these treatments usually need to be taken 3 times a day for effective pain control. The purpose of this study is to determine whether a new gabapentin tablet, which only needs to be taken once or twice a day, is safe and effective for the treatment of postherpetic neuralgia.

Detailed description

The primary study objective is to assess the relative efficacy of G-ER dosed once daily (1800 mg following the evening meal) or twice daily (600 mg AM/1200 mg PM), versus placebo in reducing the mean daily pain score from the baseline week to the end of the efficacy treatment period (Treatment Week 10) in patients with PHN. Secondary efficacy measures will include changes from baseline in mean weekly sleep interference scores, Short-Form McGill Pain Questionnaire (SF-MPQ), the Neuropathic Pain Scale (NPS), Brief Pain Inventory (BPI), Patient Global Impression of Change (PGIC), and Investigator-Rated Clinical Global Impression of Change (CGIC).

Conditions

Interventions

TypeNameDescription
DRUGGabapentin extended-release tablets

Timeline

Start date
2006-05-01
Completion
2007-07-01
First posted
2006-06-12
Last updated
2007-08-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00335933. Inclusion in this directory is not an endorsement.