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NCT00316732

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

Completed Last updated 16 October 2017
What this trial tests

trial testing IPSS Questionnaire in Prostatic Hyperplasia in 173 participants. Completed in 19 December 2006.

Timeline
25 October 2004
Primary endpoint
19 December 2006
19 December 2006

Quick facts

Lead sponsorGlaxoSmithKline
StatusCompleted
Study typeOBSERVATIONAL
Enrollment173
Start date25 October 2004
Primary completion19 December 2006
Estimated completion19 December 2006
Sites27 locations across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Eligibility, male only, with Prostatic Hyperplasia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Prostatic Hyperplasia

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00316732.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing