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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00316732
Other study ID # 103500
Secondary ID
Status Completed
Phase N/A
First received April 20, 2006
Last updated October 13, 2017
Start date October 25, 2004
Est. completion date December 19, 2006

Study information

Verified date October 2017
Source GlaxoSmithKline
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 173
Est. completion date December 19, 2006
Est. primary completion date December 19, 2006
Accepts healthy volunteers No
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who not have received any pharmacological treatment or surgical interventions for BPH (Benign Prostatic Hyperplasia).

- Patients should be prescribed dutasteride in compliance with the UK SmPC and BAUS guidelines on the treatment of BPH.

- Patients must only enter the study after the decision to prescribe dutasteride has been undertaken.

Exclusion criteria: None specified

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
IPSS Questionnaire

EQ-5D Questionnaire


Locations

Country Name City State
United Kingdom GSK Investigational Site Birmingham
United Kingdom GSK Investigational Site Bradford
United Kingdom GSK Investigational Site Bradford
United Kingdom GSK Investigational Site Bristol
United Kingdom GSK Investigational Site Colchester Essex
United Kingdom GSK Investigational Site East Kilbride
United Kingdom GSK Investigational Site Enfield Middlesex
United Kingdom GSK Investigational Site Exeter Devon
United Kingdom GSK Investigational Site Hull
United Kingdom GSK Investigational Site Ilkeston, Derbyshire
United Kingdom GSK Investigational Site Leeds
United Kingdom GSK Investigational Site Leicester Leicestershire
United Kingdom GSK Investigational Site Leytonstone London
United Kingdom GSK Investigational Site London
United Kingdom GSK Investigational Site London
United Kingdom GSK Investigational Site London
United Kingdom GSK Investigational Site Manchester Lancashire
United Kingdom GSK Investigational Site Manchester Lancashire
United Kingdom GSK Investigational Site Nottingham Nottinghamshire
United Kingdom GSK Investigational Site Plymouth Devon
United Kingdom GSK Investigational Site Sheffield
United Kingdom GSK Investigational Site Stevenage Hertfordshire
United Kingdom GSK Investigational Site Sunderland Tyne & Wear
United Kingdom GSK Investigational Site Sutton Coldfield West Midlands
United Kingdom GSK Investigational Site Tauton Somerset
United Kingdom GSK Investigational Site Torquay
United Kingdom GSK Investigational Site Wakefield

Sponsors (1)

Lead Sponsor Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

United Kingdom, 

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