ICD I27.0ORPHA:422PAH

Pulmonary Arterial Hypertension

Pulmonary arterial hypertension is a rare, progressive condition causing high blood pressure in the arteries supplying the lungs, leading to right heart failure. It predominantly affects women. While there is no cure, a growing number of targeted therapies can slow progression and improve symptoms.

526
Articles
1086
Trials (65 AU)
Updated
26 March 2026
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Common Questions

What is Pulmonary Arterial Hypertension?

Pulmonary arterial hypertension is a rare, progressive condition causing high blood pressure in the arteries supplying the lungs, leading to right heart failure. It predominantly affects women. While there is no cure, a growing number of targeted therapies can slow progression and improve symptoms.

How many clinical trials are available for Pulmonary Arterial Hypertension?

RareWays currently indexes 1086 clinical trials for Pulmonary Arterial Hypertension, of which 190 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Pulmonary Arterial Hypertension come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.