Pharmacovigilance Study To Evaluate Safety Of AVODART In Subjects With Benign Prostate Hyperplasia

NCT00593593 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2008-10-15

No results posted yet for this study

Summary

This study has 4 phases: screening phase (visit 1), treatment phase (visit 2 - 6 mths after treatment initiation), and end of treatment phase (visit 3 - end of year 1). Only in the case a serious adverse event (SAE) arises, will there be a follow up phase (visit 4).

Conditions

  • Benign Prostatic Hyperplasia

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials, MD · GlaxoSmithKline

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-12-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00593593 on ClinicalTrials.gov