Idiopathic pulmonary arterial hypertension

MONDO:0001999

A sporadic form of pulmonary arterial hypertension (PAH) characterized by elevated pulmonary arterial resistance leading to right heart failure. IPAH is progressive and potentially fatal and not associated with an underlying condition or family history of PAH. The etiology is unknown.

Also known as: IPAH, idiopathic pulmonary arterial hypertension, primary pulmonary arterial hypertension, primary pulmonary hypertension

64 clinical trials for this condition and its sub-types, 15 tagged with Idiopathic pulmonary arterial hypertension itself.

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Where it sits in the disease tree

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↑ Idiopathic disease (1285) ↑ Pulmonary arterial hypertension (208) ↑ Chronic pulmonary heart disease (18)

Including sub-types (64) Tagged with Idiopathic pulmonary arterial hypertension (15)

Trials to join now! 6 Not yet finished but already full! 1 Completed 6 Terminated 2

Virtual reality workouts tested for rare lung condition

Symptom relief By invitation only

This study tests whether exercise delivered through immersive virtual reality can improve physical performance, muscle strength, fatigue, and quality of life in 32 adults with idiopathic pulmonary arterial hypertension. Participants will do virtual reality exercises and be measur…

Sponsor: Istanbul University - Cerrahpasa • Aim: Symptom relief

Last updated Jun 27, 2026 12:26 UTC

Idiopathic pulmonary arterial hypertension

Where it sits in the disease tree

Virtual reality workouts tested for rare lung condition