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AVODART(Dutasteride) Post-marketing Surveillance(PMS) — AVO PMS  

Benign Prostatic Hyperplasia Clinical Trial

Official title:
An Open Label, Multi-centre, Non-interventional Post-marketing Surveillance to Monitor the Safety and/or Efficacy of AVODART(Dutasteride) Administered in Korean BPH(Benign Prostatic Hyperplasia) Patients According to the Prescribing Information

Clinical Trial Summary

An open label, multi-centre, non-interventional post-marketing surveillance to monitor the safety and/or efficacy of AVODART administered in Korean BPH patients according to the prescribing information

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01299571
Study type Observational
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date December 2004
Completion date July 2010
View Details
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