NCT Number: NCT00396175
Effects of Finasteride on Serum Prostate-Specific Antigen (0906-111)
A clinical study to collect additional data in order to characterize the reduction in PSA with finasteride 1 mg, and its reversibility in men with androgenetic alopecia between the ages of 40 to 60 years.
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Notify MeKey information
Conditions
Age range
40 year–60 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 3
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Men 40 to 60 years of age, and in good general physical and mental health, with androgenetic alopecia
Exclusion criteria
- History of previous bladder surgery, acute urinary retention, urethral strictures, repeated urethral catheterizations, repeated urinary tract infections, or active urinary tract infections
- History of treatment with finasteride (PROSCAR or PROPECIA) or hypersensitivity to any component of finasteride.
Treatment and study plan
Comparator : placebo (unspecified) / Duration of Treatment : 48 Weeks
DrugPrimary outcomes
-
Serum Prostatic Specific Antigen (PSA) after 48 weeks of treatment
Secondary outcomes
-
Reversibility of effects on Serum Prostatic Specific Antigen (PSA) after 24 weeks off drug
Sponsors and collaborators
Lead sponsor
Organon and Co
Industry
Registry information
Official study title
A Double-Blind, Placebo-Controlled, Multicenter Study To Examine the Effects of Finasteride 1 MG on Serum Prostate-Specific Antigen in Men With Androgenetic Alopecia
Important dates
- Study start
- 1998
- Primary completion
- 2000
- First posted
- Nov 6, 2006
- Registry last updated
- Feb 17, 2022
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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