Actively Recruiting
China Pulmonary Vascular Disease Intervention Diagnosis and Management Study-A Quality Control on Right Heart Catheterization
Led by China-Japan Friendship Hospital · Updated on 2025-05-21
10000
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to improve the quality control of right heart catheterization (RHC) procedures across multiple pulmonary hypertension centers in China. It focuses on patients who are undergoing RHC for the first time due to breathlessness or suspected pulmonary hypertension. Historically, limitations in equipment and expertise have restricted RHC use in China, and this study seeks to support better diagnosis and management of pulmonary vascular diseases by collecting detailed data from many centers. The study is observational and does not involve any treatment or intervention. It is conducted at around 30 pulmonary hypertension centers across China, enrolling patients aged 14 years and older who have RHC performed for diagnostic reasons. Researchers will collect baseline data, hemodynamic measurements from RHC, diagnostic classifications, and treatment plans. Patients will continue their routine care and follow-up at their centers while data are gathered according to the study protocol. Participants will be monitored through regular follow-ups, and all collected data will be anonymized and entered into a secure electronic system. The study team will oversee data quality and perform statistical analysis. The main outcome measured is all-cause death within 3 months, with additional assessments including diagnosis type and all-cause death at 1 year. The study started in 2018 and will continue until the end of 2030, tracking patient outcomes over time.
CONDITIONS
Brief Title
China Pulmonary Vascular Disease Intervention Diagnosis and Management Study-right Heart Catheterization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who underwent right heart catheterization for the first time due to dyspnea or suspected pulmonary hypertension
- Age 14 years or older
You will not qualify if you...
- Missing vital data
- Did not sign informed consent or did not agree to follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 1 day
Participants undergo right heart catheterization to collect baseline hemodynamic data and diagnostic classification for pulmonary hypertension.
1 visit (in-person)
Duration - Up to 1 year
Participants who undergo routine care are observed with follow-up data collected at their respective centers to monitor health outcomes.
Follow-up visits according to routine clinical care over 1 year
Trial Site Locations
Total: 1 location
1
China-Japan Friendship Hospital
Beijing, China
Actively Recruiting
Research Team
Z
Zhenguo Zhai
Y
Yu Zhang, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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