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A Study Evaluating Botulinum Toxin Type A in Subjects With Postherpetic Neuralgia

Postherpetic Neuralgia Clinical Trial

Clinical Trial Summary

4-month study including a 30-day baseline phase

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00168441
Study type Interventional
Source Allergan
Contact
Status Completed
Phase Phase 2
Start date June 2004
Completion date June 2005
View Details
See also
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