Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 4 Interventional

A Multicenter, Double-blind Study to Evaluate the Effect of Pretreatment With a Daily Dose of Sildenafil on the As-Needed Efficacy of Viagra in Men With Erectile Dysfunction and Type 2 Diabetes

ClinicalTrials.gov ID: NCT00645268

Public ClinicalTrials.gov record NCT00645268. 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 Oct 24, 2026, 5:12 PM EDT

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

Official title

A Multicenter, Double-blind Study to Evaluate the Effect of Pretreatment With a Daily Dose of Viagra® (Sildenafil Citrate) on the PRN Efficacy of Viagra in Men With Erectile Dysfunction and Type 2 Diabetes

Brief summary

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

To determine the effect on erectile function in a population of type 2 diabetic men with erectile dysfunction who have undergone the following treatment regimen: pre-treatment with a daily dose of double-blind sildenafil versus placebo for 4 weeks (Phase I) followed by an as-needed, flexible-dose, open-label treatment phase with sildenafil for 12 weeks (Phase II). To assess safety and tolerability of this dosing regimen and to investigate its effects on endothelial function and subject's responses to the Self-Esteem And Relationship (SEAR) questionnaire.

Study identification

NCT ID
NCT00645268
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
35 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
Dec 2002 (Type not available)
Primary completion
Not listed
Completion
Jan 2004 (Actual)
Last update posted
Feb 1, 2021

2002 – 2004

United States locations

U.S. sites
28
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Pfizer Investigational Site Huntsville Alabama 35801 —
Pfizer Investigational Site Phoenix Arizona 85006 —
Pfizer Investigational Site Beverly Hills California 90212 —
Pfizer Investigational Site Duarte California 91010 —
Pfizer Investigational Site La Jolla California 92037 —
Pfizer Investigational Site La Jolla California 92093 —
Pfizer Investigational Site Laguna Woods California 92653 —
Pfizer Investigational Site Los Angeles California 90048 —
Pfizer Investigational Site San Diego California 92161 —
Pfizer Investigational Site Norwalk Connecticut 06850 —
Pfizer Investigational Site Waterbury Connecticut 06708 —
Pfizer Investigational Site New Albany Indiana 47150 —
Pfizer Investigational Site Overland Park Kansas 66211 —
Pfizer Investigational Site New Orleans Louisiana 70112 —
Pfizer Investigational Site Baltimore Maryland 21224 —
Pfizer Investigational Site Baltimore Maryland 21287 —
Pfizer Investigational Site Boston Massachusetts 02215 —
Pfizer Investigational Site Minneapolis Minnesota 55416 —
Pfizer Investigational Site Richmond Heights Missouri 63117 —
Pfizer Investigational Site St Louis Missouri 63104 —
Pfizer Investigational Site Buffalo New York 14209 —
Pfizer Investigational Site Medford Oregon 97504 —
Pfizer Investigational Site Portland Oregon 97201 —
Pfizer Investigational Site San Antonio Texas 78217 —
Pfizer Investigational Site San Antonio Texas 78229-3894 —
Pfizer Investigational Site Kirkland Washington 98034 —
Pfizer Investigational Site Tacoma Washington 98023 —
Pfizer Investigational Site Tacoma Washington 98405 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00645268, 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 Feb 1, 2021 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00645268 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →