[S,S]-Reboxetine Long Term Safety Study In Post-Shingles Pain.

NCT ID: NCT00354094

Last Updated: 2007-11-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE2

Total Enrollment

600 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-11-30

Study Completion Date

2007-10-31

Brief Summary

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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.

Detailed Description

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Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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[S,S]-Reboxetine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients must have pain present for more than 3 months after healing of the shingles skin rash.
* Patients at screening must have a score of \>/=40mm on the pain visual analogue scale.

Exclusion Criteria

* Patients with significant hepatic impairment.
* Patients with other severe pain, that may impair the self-assessment of pain due to postherpetic neuralgia (pain after shingles).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Tampa, Florida, United States

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West Palm Beach, Florida, United States

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Greensboro, North Carolina, United States

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Fargo, North Dakota, United States

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Cumberland, Rhode Island, United States

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San Antonio, Texas, United States

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Buenos Aires, Buenos Aires, Argentina

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Buenos Aires, , Argentina

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Buenos Aires, , Argentina

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Buenos Aires, , Argentina

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Greater Sudbury, Ontario, Canada

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Greater Sudbury, Ontario, Canada

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Greater Sudbury, Ontario, Canada

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Toronto, Ontario, Canada

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Montreal, Quebec, Canada

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Viña del Mar, Región de Valparaíso, Chile

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Santiago, RM, Chile

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Split, , Croatia

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Hyderabad, Andhra Pradhesh, India

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Chandigarh, Punjab, India

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Bangalore, , India

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Chennai, , India

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Hyderabad, , India

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New Delhi, , India

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New Delhi, , India

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Kaunas, , Lithuania

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Klaipėda, , Lithuania

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Panevezys, , Lithuania

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Šiauliai, , Lithuania

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Mérida, Yucatán, Mexico

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Sopot, , Poland

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Ourense, OURENSE, Spain

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Stockholm, , Sweden

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Bexhill-on-Sea, East Sussex, United Kingdom

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Addlestone, SURREY, United Kingdom

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Alcester, , United Kingdom

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East Sussex, , United Kingdom

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London, , United Kingdom

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London, , United Kingdom

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London, , United Kingdom

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Countries

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United States Argentina Canada Chile Croatia India Lithuania Mexico Poland Spain Sweden United Kingdom

Related Links

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Other Identifiers

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A6061030

Identifier Type: -

Identifier Source: org_study_id