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Recruiting Observational

China Pulmonary Vascular Disease Intervention Diagnosis and Management Study-right Heart Catheterization

NCT06954727 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2018-01-01
Last updated
2025-05-21

Condition(s) studied

Pulmonary HypertensionPulmonary Embolism (Diagnosis)Pulmonary Arterial HypertensionRight Heart Catheterization

Investigational drug(s) / intervention(s)

No intervention; Observational study

No intervention; Observational study: No intervention; observational study

Study summary

Right heart catheterization(RHC) plays a crucial role in the diagnosis and treatment of pulmonary vascular diseases(PVD). In China, the lack of equipment and technical expertise has historically limited the implementation of RHC, thereby greatly restricting the diagnosis and treatment of RVD. In recent years, with improvements in these issues, more hospitals have acquired the capability to perform RHC. The purpose of this study is to conduct quality control of RHC across multiple pulmonary hypertension(PH) centers in China. The study population consists of patients who underwent RHC for the first time due to dyspnea or suspected PH. This study retrospectively and prospectively collects multicenter RHC data, with the main quality control contents including indications for the procedure, collection and analysis of hemodynamic data, diagnosis and treatment, and long-term management of patients.

Eligibility

Sex
ALL
Min age
14 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients who underwent right heart catheterization for the first time due to dyspnea or suspected pulmonary hypertension * Age ≥14 years old Exclusion Criteria: * Vital data missing * Did not sign informed consent or did not agree to follow-up

Primary outcome measure(s)

  • 3-month all cause death — 3 month
    3-month all cause death

Trial sites (1)

FacilityCityRegionStatus
China-Japan Friendship Hospital Beijing China Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06954727 on ClinicalTrials.gov ↗ ← All trials in China