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NCT07453030Possibly a fitNot yet recruiting

Selexipag for schistosomiasis-related pulmonary hypertension

Pulmonary Arterial Hypertension (PAH)

Part of Infections, Lungs & breathing clinical trials.

This study looks at the long-term effects of a medicine called selexipag on people with pulmonary hypertension caused by schistosomiasis, a parasitic infection. It aims to see if selexipag improves outcomes compared to standard care.

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

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

Who can take part

  • You must be 18 years or older.
  • You must have a confirmed diagnosis of pulmonary hypertension linked to schistosomiasis, proven by a heart catheter test.
  • You must have evidence of schistosomiasis infection, such as a history of the infection and liver or spleen changes seen on an ultrasound.
  • You must have received treatment for schistosomiasis in the past.
  • Your condition must be stable, meaning no serious heart issues or worsening symptoms in the last 12 weeks.
  • You must be in WHO functional class I to III (able to do some activity without severe symptoms), and be on stable PAH-specific medication like a PDE5 inhibitor or ERA for at least 12 weeks.

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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