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Active, not recruiting Observational

Clinical Characteristics and Outcomes of Patients With Pulmonary Hypertension Associated Right Heart Failure

NCT06023134 · tracked via the Priya Life Science China tracker
Sponsor
Jingyi Ren
Phase
Observational
Started
2015-01-01
Last updated
2025-02-18

Condition(s) studied

Right Heart FailurePulmonary Hypertension

Investigational drug(s) / intervention(s)

EchocardiographyRight heart catheterization

Echocardiography: Echocardiography will be used for specific right ventricular measurements or findings: TAPSE, TAPSE:PASP ratio, tissue Doppler velocity at lateral tricuspid annulus, fractional area change, right ventricular strain, right ventricular hypertrophy, right atrial size, volumes, ejection fraction, tricuspid and pulmonary regurgitation, inferior vena cava diameter and collapsibility, shift of interventricular septum, further assisting the diagnosis of RHF.

Right heart catheterization: Right heart catheterization is the "gold standard" for the diagnosis of PH. It also allows for direct measurement of intracardiac and pulmonary pressures, as well as cardiac output, and is commonly used to estimate right ventricular preload and afterload.

Study summary

The study aims to describe the clinical characteristics and clarify the predictors of the short- and long-term outcomes of RHF patients, further assist the diagnosis, risk stratification and treatment of RHF.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Aged ≥18 years at the time of consent 2. Acceptation of right heart catheterization examination 3. Able to perform the entire protocol Exclusion Criteria: 1. Life expectancy of less than 1 year based on the investigator's clinical judgment 2. Pregnant or nursing 3. Malignancy 4. Planned to undergo heart transplantation or device implantation 5. Acute coronary syndrome, uncontrolled severe arrhythmia and shock.

Primary outcome measure(s)

  • Time to first event of adjudicated CV death mortality or adjudicated HHF — 24 weeks
    The composite primary endpoint for this trial is the time to first event of adjudicated CV death or adjudicated hospitalization for heart failure (HHF) in patients with right heart failure.

Trial sites (1)

FacilityCityRegionStatus
China-Japan Friendship Hospital Beijing Beijing Municipality
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 NCT06023134 on ClinicalTrials.gov ↗ ← All trials in China