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Pulmonary arterial hypertension (PAH) is a rare and incurable disease affecting people of all ages. It is characterized by obstructive remodeling of the small pulmonary arteries, responsible for an in...
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Lead Sponsor
Poitiers University Hospital
NCT07120789 · Pulmonary Arterial Hypertension (PAH), Pulmonary Arterial Hypertension (PAH) (WHO Group 1 PH), and more
NCT01347216 · Pulmonary Arterial Hypertension (PAH), Pulmonary Hypertension (PH)
NCT07368088 · Pulmonary Arterial Hypertension (PAH), Premature Infants
NCT07266519 · Pulmonary Arterial Hypertension (PAH)
NCT07245680 · Pulmonary Arterial Hypertension (PAH), Comorbidities, and more
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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