Efficacy of Ventavis Used in Real-life Setting.

NCT01355380 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 55

Last updated 2017-10-17

No results posted yet for this study

Summary

This is a registry of patients diagnosed with pulmonary arterial hypertension, scheduled for treatment with Ventavis.

Typical clinical measures and quality of life will be prospectively followed in 12 months period.

Conditions

Interventions

DRUG

Inhaled iloprost (Ventavis, BAYQ6256)

Patients treated with inhaled iloprost (Ventavis) 2.5 or 5 micrograms 6-9 times daily

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-05
Primary Completion
2016-04-28
Completion
2016-09-22

Countries

  • Poland

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Entities

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 NCT01355380 on ClinicalTrials.gov