Postherpetic Neuralgia Clinical Trial
Official title:
An Open-Label Study Of The Use Of Topical Lidocaine (2.5%)/Prilocaine (2.5%) Cream As Pre-Treatment For NGX-4010 In Subjects With Postherpetic Neuralgia (PHN)
This study is an open-label multi-center to evaluate the tolerability of treatment with
NGX-4010 use with pre-patch topical application of a topical anesthetic cream. This is an
open-label study. No hypothesis testing will be performed.
Eligible subjects will have PHN and a level of pain at an intensity level deemed appropriate
for open-label treatment with NGX-4010, as judged by the Investigator. Painful areas of up
to a maximum of 1000 cm2 will be pre-treated with lidocaine (2.5%)/prilocaine (2.5%) cream
for 60 minutes followed by a single, 60-minute application of NGX-4010. Subjects may be on
chronic pain medication regimens, but currently will not be using any topical pain
medications on the affected areas, such as non-steroidal anti-inflammatory drugs, menthol,
methyl salicylate, local anesthetics including Lidoderm® (lidocaine patch 5%), steroids or
capsaicin.
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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