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Safety And Efficacy Of Lyrica (Regulatory Post Marketing Commitment Plan) — RAINBOW  

Neuralgia Clinical Trial

Official title:
DRUG USE INVESTIGATION OF LYRICA(REGULATORY POST MARKETING COMMITMENT PLAN)

Clinical Trial Summary

The objective of this Investigation is to evaluate the safety and efficacy of 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

All the patients whom an investigator prescribes the first Lyrica® should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolled into the investigation at random. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01256593
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date February 5, 2011
Completion date July 31, 2017
View Details
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