ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A 17-Week Trial To Assess Pregabalin For The Treatment Of Nerve Pain Due To Spinal Cord Injury

ClinicalTrials.gov ID: NCT00407745

Public ClinicalTrials.gov record NCT00407745. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 27, 2026, 7:25 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 17-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Trial Of Pregabalin For The Treatment Of Chronic Central Neuropathic Pain After Spinal Cord Injury

Study identification

NCT ID
NCT00407745
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Enrollment
220 participants

Conditions and interventions

Interventions

  • placebo Drug
  • pregabalin Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2006
Primary completion
Jan 31, 2011
Completion
Jan 31, 2011
Last update posted
Jan 24, 2021

2007 – 2011

United States locations

U.S. sites
22
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Pfizer Investigational Site Phoenix Arizona 85016
Pfizer Investigational Site Phoenix Arizona 85027
Pfizer Investigational Site Phoenix Arizona 85050
Pfizer Investigational Site Fresno California 93710
Pfizer Investigational Site Napa California 94558
Pfizer Investigational Site Northridge California 91324
Pfizer Investigational Site Pasadena California 91105
Pfizer Investigational Site Miami Florida 33125
Pfizer Investigational Site Miami Florida 33136
Pfizer Investigational Site Orlando Florida 32806
Pfizer Investigational Site Indianapolis Indiana 46250
Pfizer Investigational Site Overland Park Kansas 66211
Pfizer Investigational Site Detroit Michigan 48201
Pfizer Investigational Site New York New York 10029
Pfizer Investigational Site White Plains New York 10605
Pfizer Investigational Site Winston-Salem North Carolina 27103
Pfizer Investigational Site Bellevue Ohio 44811
Pfizer Investigational Site Johnstown Pennsylvania 15904
Pfizer Investigational Site Philadelphia Pennsylvania 19107
Pfizer Investigational Site Dallas Texas 75246
Pfizer Investigational Site Charleston West Virginia 25301
Pfizer Investigational Site Charleston West Virginia 25304

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00407745, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 24, 2021 · Synced Apr 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00407745 live on ClinicalTrials.gov.

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