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A 13-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, Parallel-Group Study To Evaluate The Efficacy, Safety And Tolerability Of Pregabalin (150-600 Mg/Day) Using A Flexible Dosing Schedule In The Treatment Of Subjects With Central Post-Stroke Pain (CPSP)

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A 13-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, Parallel-Group Study To Evaluate The Efficacy, Safety And Tolerability Of Pregabalin (150-600 Mg/Day) Using A Flexible Dosing Schedule In The Treatment Of Subjects With Central Post-Stroke Pain (CPSP)

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 10 Feb 2021

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At a glance

  • Drugs Pregabalin (Primary)
  • Indications Neuropathic pain
  • Focus Therapeutic Use
  • Sponsors Pfizer; Viatris Inc

    • Most Recent Events

    • 13 Apr 2010 Results presented at the 62nd Annual Meeting of the American Academy of Neurology.
    • 29 Sep 2008 Actual patient number (220) added as reported by ClinicalTrials.gov.
    • 22 Sep 2008 Status changed from recruiting to completed as reported by ClinicalTrials.gov.

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