Safety Follow-up Study of Inhaled Iloprost in Patients With Pulmonary Hypertension

NCT00185315 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2010-04-20

No results posted yet for this study

Summary

The aim of this study is to monitor long-term safety and tolerability of iloprost aerosol inhalation therapy in patients suffering from pulmonary hypertension.

Conditions

  • Hypertension, Pulmonary

Interventions

DRUG

Ventavis (Iloprost, BAYQ6256)

Inhaled iloprost

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
71 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-02-29
Completion
2005-08-31

Countries

  • Belgium
  • France
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Spain

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00185315 on ClinicalTrials.gov