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NCT04206852Recruiting

Safety and Efficacy of Balloon Pulmonary Angioplasty in China

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

Balloon pulmonary angioplasty (BPA) is a potential treatment for patients with pulmonary artery stenosis, including non-operable patients with chronic thromboembolic pulmonary hypertension (CTEPH), takayasu arteritis and fibrosis mediastinitis. The aim of this study was to evaluate the safety and efficacy of BPA in CTEPH and patients not amenable to pulmonary endarterectomy(PEA) or suffered from persistent CTEPH after PEA, , takayasu arteritis and fibrosis mediastinitis.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
26 Oct 2019
Start date
11 May 2018
Primary completion date
11 May 2065
Lead sponsor
Chinese Pulmonary Vascular Disease Research Group
NCT number
NCT04206852

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 11 May 2018 to the primary completion date, 11 May 2065
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients unwilling or unable to provide written consent for participation in the study.
  • Impossible to follow up.

Who the study is looking for

  • diagnosed with CTEPH according to ESC Guidelines (1) Mean PAP ≥ 25mmHg at rest; or if mean PAP \< 25mmHg at rest, have exercise limitations from chronic thromboembolic disease (2)Abnormal ventilation perfusion lung scanning (VQ) scan, pulmonary angiogram, computer tomographic pulmonary angiogram, or magnetic resonance pulmonary angiogram confirming chronic thromboembolic disease as recommended by standard guidelines
  • Treatment with anticoagulation for ≥ 3 months before diagnosis of CTEPH
  • Not amenable to pulmonary endarterectomy
  • Willing to provide informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Chinese Academy of Medical Sciences, Fuwai Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
center of pulmonary vascular disease, Fuwai hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.