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Real world study on the changes of pulmonary perfusion in patients with chronic thromboembolic pulmonary hypertension treated with percutaneous balloon pulmonary angioplasty versus targeted drug therapy

Real world study on the changes of pulmonary perfusion in patients with chronic thromboembolic pulmonary hypertension treated with percutaneous balloon pulmonary angioplasty versus targeted drug therapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034995
Enrollment
Unknown
Registered
2020-07-27
Start date
2019-06-01
Completion date
Unknown
Last updated
2020-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pulmonary hypertension

Interventions

BPA:BPA
Target Drug:Target Drug
BPA+Target Drug:BPA+Target Drug

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. It meets the diagnostic criteria of CTEPH, multidisciplinary assessment is not suitable for PEA treatment, and WHO cardiac function grades II to III; 2. Aged 20 to 80 years old; 3. Mean pulmonary artery pressure 25 to 60 mmHg and pulmonary artery wedge pressure (PAWP) <=15 mmHg; 4. At least 3 months of standard anticoagulant therapy (INR was controlled at 1.5–3.0 for warfarin); 5. Written informed consent was provided to fully explain the consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Previous BPA treatment; 2. Use vasodilators within 4 weeks before right heart catheterization; 3. Combined with other diseases that can cause pulmonary hypertension; 4. Pregnancy or breastfeeding; 5. Contraindications to targeted drugs or contrast agents; 6. Researchers think it is not suitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
pulmonary perfusion quantitative indexes;:right heart catheterization indexes;echocardiography indexes;Cardiopulmonary exercise testing indexes;N-terminal pro-Brain Natriuretic Peptide;

Secondary

MeasureTime frame
6-minute walk distance;Borg dyspnea indexes;WHO functional class;Quality of life;

Countries

China

Contacts

Public ContactCheng Hong

The First Affiliated Hospital of Guangzhou Medical University

gyfyyhc@126.com+86 13640815889

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026