Viewing Study NCT00316732


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Study NCT ID: NCT00316732
Status: COMPLETED
Last Update Posted: 2017-10-16
First Post: 2006-04-20
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Observational AVODART (Dutasteride) Study In Benign Prostatic Hyperplasia Subjects - OASIS
Sponsor: GlaxoSmithKline
Organization:

Study Overview

Official Title: Observational Sutdy to Assess the Effectiveness of Avodart in Subjects With Benign Prostatic Hyperplasia in Day to Day Clinical Practice
Status: COMPLETED
Status Verified Date: 2017-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: