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NCT07356375Possibly a fitNot yet recruiting

Switching from inhaled iloprost to selexipag pill for pulmonary hypertension

Pulmonary Arterial Hypertension (PAH)

Treatments studied

Part of Lungs & breathing clinical trials.

This study looks at how patients feel and how well they stick to treatment when switching from an inhaled medication (iloprost) to a pill (selexipag) for pulmonary arterial hypertension (high blood pressure in the lungs). If you are already switching, your experiences can help doctors understand the benefits and challenges of this change.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
32 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 or older.
  • You have pulmonary arterial hypertension (PAH)—a type of high blood pressure in the lungs—confirmed by a heart test.
  • You have been using inhaled iloprost (Ventavis) as part of your regular care.
  • Your doctor has decided to switch you from inhaled iloprost to the pill selexipag (Uptravi).
  • You are able to answer questionnaires about how you feel and give written consent to participate.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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