Status:

COMPLETED

A Randomized Double Blind, Placebo Controlled Balanced 4-Way Crossover Study To Assess The Efficacy Of Single Oral Doses

Lead Sponsor:

Pfizer

Conditions:

Impotence

Eligibility:

MALE

18-65 years

Phase:

PHASE2

Brief Summary

The primary aim of this study is to assess how effective PF-00592379 is in restoring penile erections in patients with erectile dysfunction. Patients will attend for 4 treatment visits where they will...

Eligibility Criteria

Inclusion

  • Erectile dysfunction, previous good response to an oral treatment for erectile dysfunction.

Exclusion

  • Patients with high blood pressure or certain heart conditions (e.g. angina, heart failure), regardless of whether treated or not.
  • Patients on nitrates or alpha-blocker medications.

Key Trial Info

Start Date :

January 1 2006

Trial Type :

INTERVENTIONAL

End Date :

Estimated Enrollment :

32 Patients enrolled

Trial Details

Trial ID

NCT00273416

Start Date

January 1 2006

Last Update

August 24 2006

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Pfizer Investigational Site

Oslo, Norway, 0277

2

Pfizer Investigational Site

Belfast, Northern Ireland, United Kingdom, BT9 6AD