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Safety and Efficacy of Gabapen for Pediatric (Regulatory Post Marketing Commitment Plan)

Epilepsies, Partial Clinical Trial

Official title:
Special Investigation Of Gabapen For Pediatric (Regulatory Post Marketing Commitment Plan)

Clinical Trial Summary

This investigation aims to understand the following issues in pediatric patients, as well as to assess the need of a special investigation and a post-marketing clinical study: - The frequency of treatment related adverse events. - The frequency of efficacy assessment. - Treatment related unlisted adverse events in Japanese Package Insert. - Risk factors likely to affect the frequency of treatment related adverse event.

Clinical Trial Description

All the patients whom an investigator prescribes the first gabapentin 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 NCT01441401
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date December 2011
Completion date September 2014
View Details
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