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Terminated Phase 2 Interventional Results available

The "Power 15 Study": Safety Study of Inhalation of Ventavis With the Power Disc-15 Setting

ClinicalTrials.gov ID: NCT00467896

Public ClinicalTrials.gov record NCT00467896. 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, 3:14 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 Comparison of Safety and Inhalation Times of Ventavis (Iloprost) Inhalation Solution Delivered by I-Neb Utilizing Power Disc-6 and Power Disc-15 "Power 15 Study"

Brief summary

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

A Comparison of Safety and Inhalation Times of Ventavis (iloprost) Inhalation Solution delivered by I-Neb Utilizing Power Disc-6 and Power Disc-15 "Power 15 Study"

Study identification

NCT ID
NCT00467896
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Actelion
Industry
Enrollment
62 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Sep 2006 (Type not available)
Primary completion
Nov 2010 (Actual)
Completion
Jun 2011 (Actual)
Last update posted
Apr 4, 2013

2006 – 2011

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Pulmonary Associates Phoenix Arizona 85006 —
UCSD Medical Center, Thorton Hospital La Jolla California 92037 —
University of Iowa Hospital and Clinics Iowa City Iowa 52242 —
Ochsner Clinic Foundation New Orleans Louisiana 70112 —
University of Maryland Hospital Baltimore Maryland 21201 —
Columbia University Medical Center New York New York 10032 —
New York Presbyterian Hospital New York New York 10032 —
Duke University Medical Center Durham North Carolina 27710 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
Baylor College of Medicine Houston Texas 77030 —
Diagnostic Research Group San Antonio Texas 78229 —
Aurora Medical Group - Cardiovascular Services Milwaukee Wisconsin 53215 —

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 NCT00467896, 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 Apr 4, 2013 · 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 NCT00467896 live on ClinicalTrials.gov.

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