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Completed Phase 2 Interventional

Inhaled Iloprost in Adults With Abnormal Pulmonary Pressure and Associated With Idiopathic Pulmonary Fibrosis

ClinicalTrials.gov ID: NCT00109681

Public ClinicalTrials.gov record NCT00109681. 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 19, 2026, 1:15 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 Randomized, Double-blind, Placebo-Controlled Phase II Study to Evaluate the Safety and Pilot Efficacy of Iloprost Inhalation Solution in Adults With Abnormal Pulmonary Arterial Pressure and Exercise Limitation Associated With Idiopathic Pulmonary Fibrosis (IPF)

Brief summary

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

The primary purpose of this study is to determine whether iloprost inhalation solution is safe in subjects with idiopathic pulmonary fibrosis (IPF) and elevated pulmonary arterial pressure. The secondary purpose is to evaluate the effectiveness of this treatment in subjects with this disease.

Study identification

NCT ID
NCT00109681
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Actelion
Industry
Enrollment
50 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 85 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
Apr 2005 (Type not available)
Primary completion
Oct 2006 (Actual)
Completion
Oct 2006 (Actual)
Last update posted
Feb 15, 2010

2005 – 2006

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
UCLA School of Medicine Los Angeles California 90095 —
University of California, San Diego San Diego California 92037 —
University of California, San Francisco San Francisco California 94143 —
University of Miami Miami Florida 33136 —
The University of Chicago Chicago Illinois 60637 —
University of Iowa College of Medicine Iowa City Iowa 52242 —
Tulane University New Orleans Louisiana 70112 —
University of Michigan Health System Ann Arbor Michigan 48109 —
Mayo Clinic Rochester Rochester Minnesota 55905 —
Mount Sinai Medical Center New York New York 10029 —
Duke University Medical Center Durham North Carolina 27710 —
University of Pittsburgh School of Medicine Pittsburgh Pennsylvania 15213 —
Vanderbilt University Medical Nashville Tennessee 37232 —
Baylor College of Medicine Houston Texas 77030 —
University of Texas Health Center at Tyler Tyler Texas 75708 —
Inova Research Center Church Falls Virginia 22042 —

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 NCT00109681, 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 15, 2010 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00109681 live on ClinicalTrials.gov.

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