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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00141375
Other study ID # 1008-000-202
Secondary ID
Status Completed
Phase Phase 3
First received August 30, 2005
Last updated January 9, 2008
Start date August 2002
Est. completion date January 2006

Study information

Verified date January 2008
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 132
Est. completion date January 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Must have met the inclusion criteria of the preceding double-blind BID study in central pain following spinal cord injury.

- 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.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Pregabalin


Locations

Country Name City State
Australia Pfizer Investigational Site Heidelberg Victoria
Australia Pfizer Investigational Site Little Bay New South Wales
Australia Pfizer Investigational Site NSW
Australia Pfizer Investigational Site Shenton Park Western Australia
Australia Pfizer Investigational Site St. Leonards New South Wales
Australia Pfizer Investigational Site Warrawong New South Wales
Australia Pfizer Investigational Site Woolloongabba Queensland

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety and Efficacy
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