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Safety And Efficacy In Long Term Use Of Lyrica (Regulatory Post Marketing Commitment Plan) — RAINBOW-L  

Neuropathic Pain Clinical Trial

Official title:
SPECIAL INVESTIGATION OF LONG TERM USE OF LYRICA(REGULATORY POST MARKETING COMMITMENT PLAN)

Clinical Trial Summary

The objective of this investigation is to evaluate the safety and efficacy of long term use with Lyrica in medical practice. Also, occurrence of unknown and known adverse drug reactions (ADRs) in subjects treated with Lyrica will be monitored during the survey period, and whether an additional treatment outcome investigation and/or a post-marketing clinical study is required in the future will be determined.

Clinical Trial Description

Patients who fulfill criteria below: 1. Patients who have previously enrolled in A0081261. 2. Patients who have been administered Lyrica for more than 52 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01279850
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date August 2011
Completion date July 2017
View Details
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