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Completed Phase 4 Interventional

Mild To Moderate Erectile Dysfunction Study

ClinicalTrials.gov ID: NCT00137072

Public ClinicalTrials.gov record NCT00137072. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 1:02 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Randomized, Double-Blind, Placebo-Controlled, Fixed-Dose Parallel Study of Men With Mild to Moderate Erectile Dysfunction to Evaluate the Efficacy of Viagra 8 Hours Post-Dose

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Safety/Efficacy of 100-mg Viagra at 8 hours post dose in men with mild to moderate erectile dysfunction

Study identification

NCT ID
NCT00137072
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
355 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2005
Primary completion
Not listed
Completion
Jan 31, 2006
Last update posted
Jan 31, 2021

2005 – 2006

United States locations

U.S. sites
33
U.S. states
16
U.S. cities
33
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama
Pfizer Investigational Site Homewood Alabama
Pfizer Investigational Site Hoover Alabama
Pfizer Investigational Site Huntsville Alabama
Pfizer Investigational Site Phoenix Arizona
Pfizer Investigational Site Beverly Hills California
Pfizer Investigational Site La Mesa California
Pfizer Investigational Site Newport Beach California
Pfizer Investigational Site San Diego California
Pfizer Investigational Site Aurora Colorado
Pfizer Investigational Site Middlebury Connecticut
Pfizer Investigational Site Waterbury Connecticut
Pfizer Investigational Site Gainesville Florida
Pfizer Investigational Site New Port Richey Florida
Pfizer Investigational Site South Miami Florida
Pfizer Investigational Site Tallahassee Florida
Pfizer Investigational Site Tampa Florida
Pfizer Investigational Site Fort Wayne Indiana
Pfizer Investigational Site Jeffersonville Indiana
Pfizer Investigational Site Des Moines Iowa
Pfizer Investigational Site New Orleans Louisiana
Pfizer Investigational Site Shreveport Louisiana
Pfizer Investigational Site Hattiesburg Mississippi
Pfizer Investigational Site Las Vegas Nevada
Pfizer Investigational Site Bay Shore New York
Pfizer Investigational Site Kingston New York
Pfizer Investigational Site New York New York
Pfizer Investigational Site Poughkeepsie New York
Pfizer Investigational Site Cincinnati Ohio
Pfizer Investigational Site Nashville Tennessee
Pfizer Investigational Site San Antonio Texas
Pfizer Investigational Site Lacey Washington
Pfizer Investigational Site Spokane Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00137072, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 31, 2021 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00137072 live on ClinicalTrials.gov.

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