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COMPLETED Phase 3

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

NCT00407745 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate if pregabalin relieves nerve pain associated with spinal cord injury compared to placebo (pill that contains no active medicine). This study will also evaluate the safety of pregabalin in this patient population.

Interventions

  • DRUG placebo
  • DRUG pregabalin

Study Locations (20)

California

  • Pfizer Investigational Site — Fresno
  • Pfizer Investigational Site — Napa
  • Pfizer Investigational Site — Northridge
  • Pfizer Investigational Site — Pasadena

Arizona

  • Pfizer Investigational Site — Phoenix
  • Pfizer Investigational Site — Phoenix
  • Pfizer Investigational Site — Phoenix

Florida

  • Pfizer Investigational Site — Miami
  • Pfizer Investigational Site — Miami
  • Pfizer Investigational Site — Orlando

New York

  • Pfizer Investigational Site — New York
  • Pfizer Investigational Site — White Plains

Pennsylvania

  • Pfizer Investigational Site — Johnstown
  • Pfizer Investigational Site — Philadelphia

Indiana

  • Pfizer Investigational Site — Indianapolis

Kansas

  • Pfizer Investigational Site — Overland Park

Michigan

  • Pfizer Investigational Site — Detroit

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2007-01
Est. Completion 2011-02
Phase Phase 3

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00407745

The ClinicalTrials.gov registry entry for NCT00407745 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 27 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Spinal Cord Injuries appearing as the primary indexed condition, and to 2 interventions — of which placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00407745 reports 20 study locations spanning 11 distinct geographic areas — top geographies include California, Arizona, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00407745 about?

NCT00407745 is a clinical study titled "A 17-Week Trial To Assess Pregabalin For The Treatment Of Nerve Pain Due To Spinal Cord Injury". The purpose of this study is to evaluate if pregabalin relieves nerve pain associated with spinal cord injury compared to placebo (pill that contains no active medicine). This study will also evaluate the safety of pregabalin in this patient population.

What is the current status of trial NCT00407745?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 220 participants. The study started on 2007-01. Estimated completion is 2011-02.

What conditions does trial NCT00407745 study?

This clinical trial studies the following conditions: Spinal Cord Injuries, Neuralgia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00407745?

The interventions under investigation include: placebo (DRUG), pregabalin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00407745?

This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 27 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00407745 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Indiana, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial