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Completed Phase 3 Interventional Results available

A Long Term Extension Study Evaluating Safety Of Sildenafil Citrate When Used To Treat Pulmonary Arterial Hypertension (PAH) In Children

ClinicalTrials.gov ID: NCT00159874

Public ClinicalTrials.gov record NCT00159874. 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 May 5, 2026, 7:12 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, Long-Term Extension Study to Assess Safety of Oral Sildenafil Citrate In The Treatment Of Subjects Who Have Completed Study A1481131

Study identification

NCT ID
NCT00159874
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Enrollment
234 participants

Conditions and interventions

Interventions

  • Sildenafil citrate Drug

Drug

Eligibility (public fields only)

Age range
1 Year to 17 Years
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
Dec 31, 2003
Primary completion
Nov 30, 2012
Completion
Nov 30, 2012
Last update posted
Jan 31, 2021

2004 – 2012

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Pfizer Investigational Site Palo Alto California 34304
Pfizer Investigational Site Palo Alto California 94305
Pfizer Investigational Site Stanford California 94305
Pfizer Investigational Site Aurora Colorado 80045
Pfizer Investigational Site Boston Massachusetts 02115
Pfizer Investigational Site Ann Arbor Michigan 48109
Pfizer Investigational Site St Louis Missouri 63110
Pfizer Investigational Site New York New York 10032
Pfizer Investigational Site Columbus Ohio 43205
Pfizer Investigational Site Charleston South Carolina 29425
Pfizer Investigational Site Seattle Washington 98105

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 28 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00159874, 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 May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00159874 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →