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CompletedNCT00424372

A Long-Term Study To Evaluate Safety And Efficacy Of Pregabalin For Postherpetic Neuralgia

A LONG-TERM STUDY TO EVALUATE SAFETY AND EFFICACY STUDY OF PREGABALIN IN THE TREATMENT OF POSTHERPETIC NEURALGIA.

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

Summary

To evaluate the safety of the long-term use of pregabalin.

Conditions

Interventions

TypeNameDescription
DRUGpregabalinDosage: 150-600 mg/day (75-300 mg bid), oral administration, Treatment duration: 52 weeks

Timeline

Start date
2007-01-12
Primary completion
2008-08-19
Completion
2008-08-19
First posted
2007-01-19
Last updated
2021-08-27
Results posted
2009-09-28

Locations

33 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT00424372. Inclusion in this directory is not an endorsement.

A Long-Term Study To Evaluate Safety And Efficacy Of Pregabalin For Postherpetic Neuralgia (NCT00424372) · Clinical Trials Directory