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CompletedNCT01202227

An Open-Label Long-Term Study Of Pregabalin For The Treatment Of Central Neuropathic Pain

An Open-Label Long-Term Study Of Pregabalin For The Treatment Of Central Neuropathic Pain (Post Spinal Cord Injury Pain, Post Stroke Pain, And Multiple Sclerosis Pain)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
104 (actual)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the safety of the long-term use of pregabalin at doses up to 600 mg/day in patients with central neuropathic pain (post spinal cord injury pain, post stroke pain, and multiple sclerosis pain).

Conditions

Interventions

TypeNameDescription
DRUGpregabalinPregabalin capsules taken twice a daily (150-600mg/day)

Timeline

Start date
2010-09-01
Primary completion
2012-03-01
Completion
2012-03-01
First posted
2010-09-15
Last updated
2021-01-28
Results posted
2013-05-17

Locations

26 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT01202227. Inclusion in this directory is not an endorsement.

An Open-Label Long-Term Study Of Pregabalin For The Treatment Of Central Neuropathic Pain (NCT01202227) · Clinical Trials Directory