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NCT01355380: SPHERA

Efficacy of Ventavis Used in Real-life Setting.

Completed Last updated 17 October 2017
What this trial tests

trial testing Inhaled iloprost (Ventavis, BAYQ6256) in Pulmonary Arterial Hypertension in 55 participants. Completed in 22 September 2016.

Timeline
5 August 2010
Primary endpoint
28 April 2016
22 September 2016

Quick facts

Lead sponsorBayer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment55
Start date5 August 2010
Primary completion28 April 2016
Estimated completion22 September 2016
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

18 and older, any sex, with Pulmonary Arterial Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Pulmonary Arterial Hypertension

Currently open trials in the same condition.

Other Bayer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01355380.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing