To Evaluate Long-Term Safety and Efficacy of Pregabalin in the Treatment of Neuropathic Pain After Spinal Cord Injury.

NCT ID: NCT00141375

Last Updated: 2008-01-15

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

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

132 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-08-31

Study Completion Date

2006-01-31

Brief Summary

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To evaluate long-term safety and efficacy of pregabalin in the treatment of neuropathic pain after spinal cord injury.

Detailed Description

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Conditions

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Neuropathic Pain

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Pregabalin

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Must have received study medication under double-blind conditions.

Exclusion Criteria

* Patients cannot participate if they experienced a serious adverse event during the previous double-blind BID study which was determined to be related to the study medication.
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

Little Bay, New South Wales, Australia

Site Status

Pfizer Investigational Site

St Leonards, New South Wales, Australia

Site Status

Pfizer Investigational Site

Warrawong, New South Wales, Australia

Site Status

Pfizer Investigational Site

Woolloongabba, Queensland, Australia

Site Status

Pfizer Investigational Site

Heidelberg, Victoria, Australia

Site Status

Pfizer Investigational Site

Shenton Park, Western Australia, Australia

Site Status

Pfizer Investigational Site

NSW, , Australia

Site Status

Countries

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Australia

Other Identifiers

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1008-000-202

Identifier Type: -

Identifier Source: org_study_id

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