Riociguat in Triple Therapy for Pulmonary Arterial Hypertension in Real-World Practice
- Sponsor
- Caio Júlio César dos Santos Fernandes
- Study ID
- NCT07374302
- Status
- Not Yet Recruiting
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Conditions
- Pulmonary Arterial Hypertension
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Study Details
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.
Key Dates
- First listed
- Jan 28, 2026
- Start date
- Mar 1, 2026
- Status verified
- Jan 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 15 participants (estimated)
Arms
- Arm: Riociguat Triple Therapy CohortAdult patients with pulmonary arterial hypertension receiving triple therapy who switched from a phosphodiesterase-5 inhibitor to riociguat as part of routine clinical care. The index date (T0) is defined as the date of riociguat initiation.
Primary Outcome Measure
Composite Clinical Outcome at 6 Months [ Time Frame: 6 months (24±8 weeks) after switch ]
Central Contacts
- Caio Fernandes, Principal Investigator, MD+551126615034
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