Observational AVODART (Dutasteride) Study In Benign Prostatic Hyperplasia Subjects - OASIS

NCT00316732 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 173

Last updated 2017-10-16

No results posted yet for this study

Summary

This study was designed to assess the effectiveness of dutasteride in the actual clinical practice of prostate assessment clinics in the UK in accordance with best practice over a 12-month period.

Conditions

  • Prostatic Hyperplasia

Interventions

PROCEDURE

IPSS Questionnaire

PROCEDURE

EQ-5D Questionnaire

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-10-25
Primary Completion
2006-12-19
Completion
2006-12-19

Countries

  • United Kingdom

Study Locations

More Related Trials

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 NCT00316732 on ClinicalTrials.gov