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NCT00168441 Clinical Trial

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

Postherpetic Neuralgia Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00168441
Other study ID # 191622-066
Secondary ID
Status Completed
Phase Phase 2
First received September 12, 2005
Last updated May 27, 2011
Start date June 2004
Est. completion date June 2005

Study information
Verified date May 2011
Source Allergan
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

4-month study including a 30-day baseline phase

Recruitment information / eligibility
Status Completed
Enrollment 117
Est. completion date June 2005
Est. primary completion date June 2005
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Postherpetic neuralgia for more than 3 months after the healing of a herpes zoster skin rash.

Exclusion Criteria:

- Previous use of botulinum toxin of any serotype or immunization to any botulinum toxin serotype.

Study Design

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

Related Conditions & MeSH terms

Intervention

Drug:
• Botulinum Toxin Type A

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Allergan

Outcome
Type Measure Description Time frame Safety issue
Primary Pain score
Secondary Various Quality of Life questionnaires
Secondary Reduction in area of pain/allodynia
See also
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