Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

The Efficacy and Safety of Sildenafil Citrate Used in Combination With Intravenous Epoprostenol in PAH

ClinicalTrials.gov ID: NCT00159861

Public ClinicalTrials.gov record NCT00159861. 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 22, 2026, 12:56 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

A Multinational, Multi-Center, Randomised, Double-Bind, Placebo-Controlled, Parallel Group Study to Assess the Safety and Efficacy of a Subject Optimised Dose of Sildenafil Citrate (20, 40, or 80 mg. Sildenafil Citrate TID) Based on the Toleration, When Used in Combination With Intravenous Prostacyclin( Epoprostenol) in the Treatment of Pulmonary Arterial Hypertension.

Brief summary

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

Determination of the effects of sildenafil citrate and epoprostenol when used in combination in patients with pulmonary arterial hypertension

Study identification

NCT ID
NCT00159861
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
267 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
16 Years and older
Sex
All
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
Jul 2003 (Type not available)
Primary completion
Not listed
Completion
Jan 2006 (Actual)
Last update posted
Feb 1, 2021

2003 – 2006

United States locations

U.S. sites
33
U.S. states
20
U.S. cities
24
Facility City State ZIP Site status
Pfizer Investigational Site La Jolla California 92037 —
Pfizer Investigational Site Los Angeles California 90033 —
Pfizer Investigational Site Los Angeles California 90073 —
Pfizer Investigational Site San Diego California 92103 —
Pfizer Investigational Site Torrance California 90502 —
Pfizer Investigational Site Torrance California 90509 —
Pfizer Investigational Site Denver Colorado 80220 —
Pfizer Investigational Site Denver Colorado 80262 —
Pfizer Investigational Site Chicago Illinois 60637 —
Pfizer Investigational Site Kansas City Kansas 66160 —
Pfizer Investigational Site New Orleans Louisiana 70112 —
Pfizer Investigational Site Baltimore Maryland 21287 —
Pfizer Investigational Site Boston Massachusetts 02111 —
Pfizer Investigational Site Boston Massachusetts 02114 —
Pfizer Investigational Site Ann Arbor Michigan 48109 —
Pfizer Investigational Site Rochester Minnesota 55905 —
Pfizer Investigational Site St Louis Missouri 63110 —
Pfizer Investigational Site Omaha Nebraska 68105 —
Pfizer Investigational Site Omaha Nebraska 68198-2125 —
Pfizer Investigational Site New York New York 10032 —
Pfizer Investigational Site Durham North Carolina 27710 —
Pfizer Investigational Site Cincinnati Ohio 45219 —
Pfizer Investigational Site Cincinnati Ohio 45267-0769 —
Pfizer Investigational Site Cleveland Ohio 44195 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15213 —
Pfizer Investigational Site Providence Rhode Island 02903 —
Pfizer Investigational Site Nashville Tennessee 37232-5735 —
Pfizer Investigational Site Nashville Tennessee 37232 —
Pfizer Investigational Site Houston Texas 77030 —
Pfizer Investigational Site Salt Lake City Utah 84143 —
Pfizer Investigational Site Milwaukee Wisconsin 53215 —
Pfizer Investigational Site Milwaukee Wisconsin 53226 —
Pfizer Investigational Site Milwaukee Wisconsin 53277 —

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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00159861, 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 22, 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 NCT00159861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →