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This study assesses heart function using the pressure-volume (PV) loop method in patients with idiopathic pulmonary arterial hypertension or scleroderma-associated pulmonary hypertension. It enrolled patients aged 18 and older who had received these clinical diagnoses. The study was conducted as a non-phase study and has been completed.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: * Patients 18 years or older with clinically diagnosed scleroderma or presumed/known idiopathic pulmonary hypertension. Exclusion Criteria: * Patients found to have secondary pulmonary hypertension (PH due to left heart failure) on clinical RHC. * Hemodynamically unstable patients (systolic blood pressure \< 90mmHg, vasopressor requirement). * Patients whom are unable to give consent for themselves. * Patients with RV clot or septal aneurysm will be excluded. * In order to undergo the clinical right heart catheterization procedures, pregnancy testing (urine or serum) is standard of care. * Pregnancy