Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

An Open-Label, Extension Study Evaluating the Safety, Toleration, and Efficacy of Sildenafil in Women With Sexual Arousal Disorder

ClinicalTrials.gov ID: NCT00746967

Public ClinicalTrials.gov record NCT00746967. 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 28, 2026, 1:54 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

An Open-Label, Multi-Center Extension Study To Evaluate The Safety, Toleration And Sustained Efficacy Of Oral Sildenafil Administered To Women Who Have Been Diagnosed With Female Sexual Arousal Disorder

Brief summary

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

The purpose of this study is to evaluate the safety and toleration of oral sildenafil administered as required by women with Female Sexual Arousal Disorder (FSAD) who successfully complete one of the following Pfizer-sponsored, 12-week, double-blinded clinical trials: A1481082 or A1481123. Addition of this 52-week open-label extension will increase the total duration of sildenafil exposure to 64 weeks. Sustained efficacy will also be evaluated after 3 and 6 months of open-label therapy.

Study identification

NCT ID
NCT00746967
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
267 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Jan 2003 (Type not available)
Primary completion
Not listed
Completion
Feb 2004 (Actual)
Last update posted
Feb 1, 2021

2003 – 2004

United States locations

U.S. sites
82
U.S. states
32
U.S. cities
71
Facility City State ZIP Site status
Pfizer Investigational Site Huntsville Alabama 35801 —
Pfizer Investigational Site Anchorage Alaska 99502 —
Pfizer Investigational Site Anchorage Alaska 99508 —
Pfizer Investigational Site Tucson Arizona 85712 —
Pfizer Investigational Site Tucson Arizona 85719 —
Pfizer Investigational Site Jonesboro Arkansas 72401 —
Pfizer Investigational Site Albany California 94706 —
Pfizer Investigational Site Berkeley California 94705 —
Pfizer Investigational Site Beverly Hills California 90210 —
Pfizer Investigational Site Beverly Hills California 90212 —
Pfizer Investigational Site Burbank California 91506 —
Pfizer Investigational Site Fair Oaks California 95628 —
Pfizer Investigational Site Hermosa Beach California 90254 —
Pfizer Investigational Site Oakland California 94612 —
Pfizer Investigational Site San Diego California 92103 —
Pfizer Investigational Site San Diego California 92108 —
Pfizer Investigational Site Santa Monica California 90404 —
Pfizer Investigational Site Torrance California 90505 —
Pfizer Investigational Site Aurora Colorado 80012 —
Pfizer Investigational Site Hamden Connecticut 06518 —
Pfizer Investigational Site New London Connecticut 06320 —
Pfizer Investigational Site Waterbury Connecticut 06708 —
Pfizer Investigational Site Aventura Florida 33180 —
Pfizer Investigational Site Brooksville Florida 34614 —
Pfizer Investigational Site Jensen Beach Florida 34957 —
Pfizer Investigational Site Miami Florida 33186 —
Pfizer Investigational Site New Port Richey Florida 34652 —
Pfizer Investigational Site Palm Harbor Florida 34683 —
Pfizer Investigational Site Pembroke Pines Florida 33028 —
Pfizer Investigational Site Plantation Florida 33324 —
Pfizer Investigational Site St. Petersburg Florida 33710 —
Pfizer Investigational Site Stuart Florida 34994 —
Pfizer Investigational Site Stuart Florida 34996 —
Pfizer Investigational Site West Palm Beach Florida 33409 —
Pfizer Investigational Site Atlanta Georgia 30309 —
Pfizer Investigational Site Atlanta Georgia 30342 —
Pfizer Investigational Site Marietta Georgia 30060 —
Pfizer Investigational Site Savannah Georgia 31405 —
Pfizer Investigational Site Boise Idaho 83702 —
Pfizer Investigational Site Boise Idaho 83712 —
Pfizer Investigational Site Evansville Indiana 47714 —
Pfizer Investigational Site Fort Wayne Indiana 46825 —
Pfizer Investigational Site Newburgh Indiana 47630 —
Pfizer Investigational Site Leawood Kansas 66211 —
Pfizer Investigational Site Crestview Hills Kentucky 41017 —
Pfizer Investigational Site Florence Kentucky 41042 —
Pfizer Investigational Site Metairie Louisiana 70002 —
Pfizer Investigational Site Greenbelt Maryland 20770 —
Pfizer Investigational Site Kalamazoo Michigan 49009 —
Pfizer Investigational Site Southfield Michigan 48034 —
Pfizer Investigational Site Creve Coeur Missouri 63141 —
Pfizer Investigational Site Henderson Nevada 89014 —
Pfizer Investigational Site North Las Vegas Nevada 89030 —
Pfizer Investigational Site New Brunswick New Jersey 08903 —
Pfizer Investigational Site New York New York 10021 —
Pfizer Investigational Site Poughkeepsie New York 12601 —
Pfizer Investigational Site Rochester New York 14609 —
Pfizer Investigational Site White Plains New York 10603 —
Pfizer Investigational Site Winston-Salem North Carolina 27103 —
Pfizer Investigational Site Beachwood Ohio 44122-5402 —
Pfizer Investigational Site Cincinnati Ohio 45267-0559 —
Pfizer Investigational Site Philadelphia Pennsylvania 19106 —
Pfizer Investigational Site Philadelphia Pennsylvania 19148 —
Pfizer Investigational Site Reading Pennsylvania 19606 —
Pfizer Investigational Site Reading Pennsylvania 19607-1649 —
Pfizer Investigational Site Temple Pennsylvania 19560 —
Pfizer Investigational Site West Reading Pennsylvania 19611-1499 —
Pfizer Investigational Site Providence Rhode Island 02904 —
Pfizer Investigational Site Anderson South Carolina 29621 —
Pfizer Investigational Site Memphis Tennessee 38119 —
Pfizer Investigational Site Austin Texas 78705 —
Pfizer Investigational Site Austin Texas 78758 —
Pfizer Investigational Site Dallas Texas 75231 —
Pfizer Investigational Site Houston Texas 77024 —
Pfizer Investigational Site Sandy City Utah 84070 —
Pfizer Investigational Site Charlottesville Virginia 22903 —
Pfizer Investigational Site Richmond Virginia 23294 —
Pfizer Investigational Site Renton Washington 98055 —
Pfizer Investigational Site Seattle Washington 98105 —
Pfizer Investigational Site Seattle Washington 98115 —
Pfizer Investigational Site Milwaukee Wisconsin 53209 —
Pfizer Investigational Site Cheyenne Wyoming 82001 —

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 NCT00746967, 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 28, 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 NCT00746967 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →