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Pulmonary Arterial Hypertension (PAH) in the setting of Idiopathic Pulmonary Fibrosis(IPF)is a risk factor for morbidity and mortality in the peri-lung transplant(LT) setting. Currently there is no si...
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Lead Sponsor
University of California, Los Angeles
Collaborators
NCT07365332 · Pulmonary Arterial Hypertension
NCT07218029 · Pulmonary Arterial Hypertension
NCT07572383 · Interstitial Lung Disease, Pulmonary Fibrosis
NCT06649110 · Healthy Volunteers, Pulmonary Arterial Hypertension
NCT05139719 · Progressive Fibrosing Interstitial Lung Disease (PF-ILD) / Progressive Pulmonary Fibrosis (PPF)
David Geffen School of Medicine UCLA
Los Angeles, California
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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