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OpenTrials
Completed

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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Key information

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

MK0906, finasteride / Duration of Treatment : 48 Weeks

Drug

Comparator : placebo (unspecified) / Duration of Treatment : 48 Weeks

Drug

Primary outcomes

  1. Serum Prostatic Specific Antigen (PSA) after 48 weeks of treatment

Secondary outcomes

  1. 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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