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Balloon pulmonary angioplasty (BPA) is a potential treatment for non-operable patients with chronic thromboembolic pulmonary hypertension (CTEPH). The aim of this study was to evaluate the safety and efficacy of BPA in CTEPH patients not amenable to pulmonary endarterectomy(PEA) or suffered from persistent CTEPH after PEA.
This study is a prospective, multi-center, long-term observational project to study the safety and efficacy of BPA. Clinical evaluation, including: functional capacity, 6-minutes walking test, biomarkers, cardiopulmonary exercise test, electrocardiography, echocardiography, haemodynamics, pulmonary angiography and lung scintigraphy was performed before the initiation therapy of BPA, and 3-12 months after last session of BPA. we also aim to evaluate the value of FAPI in predicting the efficacy and the prognosis of patients with CTEPH who received BPA.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
center of pulmonary vascular disease, Fuwai hospital
Beijing, China
Chinese Academy of Medical Sciences Fuwai hospital
Beijing, China
Start Date
May 11, 2018
Primary Completion Date
May 11, 2028
Completion Date
May 11, 2028
Last Updated
December 20, 2023
200
ESTIMATED participants
Balloon pulmonary angioplasty
PROCEDURE
Lead Sponsor
Chinese Pulmonary Vascular Disease Research Group
NCT06526468
NCT03388476
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