[S,S]-Reboxetine Long Term Safety Study In Post-Shingles Pain.
NCT00354094 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 600
Last updated 2007-11-08
Summary
The purpose of this study is to assess the long term (up to 2 years) safety and tolerability of \[S,S\]-Reboxetine in patients with pain after shingles.
Conditions
Interventions
- DRUG
-
[S,S]-Reboxetine
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-11-30
- Completion
- 2007-10-31
Countries
- United States
- Argentina
- Canada
- Chile
- Croatia
- India
- Lithuania
- Mexico
- Poland
- Spain
- Sweden
- United Kingdom
Study Locations
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