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QEQ Treatment Responsiveness Evaluation Study

Last updated on March 14, 2019

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Study Location
Pfizer Investigational Site
Bondi Junction, New South Wales, Australia
Contact
1-800-718-1021
Eligibility criteria
Condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Impotence
Sex
Male
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18 + years
Inclusion criteria
The factors, or reasons, that allow a person to participate in a clinical study.
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- Subjects must have documented clinical diagnosis of erectile dysfunction based on a
screening SHI-M score of dysfunction

- Subjects must be either PDE-5 inhibitor naive; i.e. have never used sildenafil,
tadalafil or vardenafil, or have been previously treated with no more than six doses
of a PDE-5 inhibitor (sildenafil, tadalafil, vardenafil) and must have taken their
last dose no less than 4 weeks prior to the screening visit

Exclusion criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
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- Subjects who are currently prescribed, taking and/or likely to be treated with
nitrates or nitric oxide donors in any form on either a regular or intermittent basis

NCT00151463
Pfizer
Completed
QEQ Treatment Responsiveness Evaluation Study

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