Non-interventional Study on Compliance of Inhaled Treatment With Ventavis in Patient With Pulmonary Hypertension

NCT01971450 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 89

Last updated 2019-03-26

No results posted yet for this study

Summary

Local, prospective, multicenter, non-comparative, non-interventional, observational study. It is planed to assess compliance of patients with PH (pulmonary hypertension) with the physician's recommendation in real practice.

Conditions

  • Hypertension, Pulmonary

Interventions

DRUG

Iloprost (Ventavis, BAYQ6256)

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-21
Primary Completion
2017-06-28
Completion
2018-04-18

Countries

  • Russia

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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 NCT01971450 on ClinicalTrials.gov