Condition: Pulmonary Arterial Hypertension · Idiopathic Pulmonary Arterial Hypertension · Pulmonary Arterial Hypertension Associated With Connective Tissue Disease (Disorder) · Sponsor: Bastiaan Driehuys
The overall study objectives outlined in this study are to derive 129Xe MRI pulmonary vascular biomarker signatures that differentiate common subtypes of PAH and to determine the ability of 129Xe MRI to longitudinally monitor disease progression and response to therapy in PAH, with the aid of additional assessments, such as labs, echocardiography, and six-minute walk distance (6MWD).
This description comes directly from the study's public registry record.
Claudia Salazar · +1 919 660 2026 · claudia.salazar@duke.edu
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| Duke University Medical Center | Durham, North Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06104228