Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Long-Term Outcomes of Selexipag in Schistosomiasis-Associated Pulmonary Arterial Hypertension

Schistosomiasis-associated pulmonary arterial hypertension is a serious condition that can lead to shortness of breath, heart failure, frequent hospitalizations, and early death. Although treatments for pulmonary arterial hypertension have improved over time, patients with this specific cause of the disease are often not included in long-term studies. Selexipag is an oral medication used to treat pulmonary arterial hypertension and is part of routine clinical care in Brazil. Its long-term effects in patients with schistosomiasis-associated pulmonary arterial hypertension are not well understood. The PROPULSE-Sch study aims to evaluate long-term clinical outcomes in patients with schistosomiasis-associated pulmonary arterial hypertension who received selexipag, compared with similar patients who did not receive this medication before it became available at the study center. This is an observational study using data from routine medical care. All treatments are prescribed by the treating physicians, and participation in the study does not change patient care. The results may help improve understanding of long-term outcomes and support treatment decisions in this population.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Caio Júlio César dos Santos FernandesUpdated: Mar 5, 2026Locations: 1
Eligibility criteria

Confirmed diagnosis of pulmonary arterial hypertension associated with schistoso... [+8]

World Health Organization (WHO) functional class IV at the index date. [+3]

Status: Not yet recruiting

Riociguat in Triple Therapy for Pulmonary Arterial Hypertension in Real-World Practice

Pulmonary arterial hypertension is a rare and serious disease that can lead to heart failure and early death despite modern treatments. Many patients are treated with a combination of medications targeting different disease pathways, but some continue to have an inadequate response. Riociguat is a medication that acts on the nitric oxide pathway and may be beneficial in patients who do not respond well to phosphodiesterase-5 inhibitors. In routine clinical practice, some patients receiving triple therapy switch from a phosphodiesterase-5 inhibitor to riociguat. The REAPPRAISED study evaluates outcomes in patients with pulmonary arterial hypertension who switched to riociguat while receiving triple therapy. This observational study uses data from routine clinical care and does not involve any experimental treatment. The results may help improve understanding of the effectiveness and safety of this treatment strategy in real-world practice.

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Caio Júlio César dos Santos FernandesUpdated: Jan 28, 2026
Eligibility criteria

Adults aged 18 years or older. [+4]

Concomitant use of phosphodiesterase-5 inhibitors and riociguat. [+2]