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A modified 4-strata risk assessment instrument in Chinese patients with pulmonary arterial hypertension based on a retrospective database

A modified 4-strata risk assessment instrument in Chinese patients with pulmonary arterial hypertension based on a retrospective database

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100857
Enrollment
Unknown
Registered
2025-04-16
Start date
2025-04-30
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

pulmonary arterial hypertension (PAH)

Interventions

Observation group:Observation study, no intervention involved

Sponsors

Fuwai Hospital Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age >= 18 years. 2) Treatment-naïve and newly diagnosed with any form of PAH through RHC at hospitalization at Fuwai Hospital from Jan 1 2018 to Dec 31 2023. 3) Baseline hemodynamics showing mPAP ?25 mmHg, PAWP?15 mmHg and PVR>3 Wood units (240 dyn·s·cm-5); 4) All variables of interest (WHO FC, 6MWD, NT-proBNP, and TAPSE and estimated sPAP in echocardiography) available at baseline. 5) At least one documented follow-up with NT-ProBNP, WHO-FC, TAPSE and sPAP or 6MWD.

Exclusion criteria

Exclusion criteria: 1) Initial diagnosis of PAH before Jan 1, 2018 2) Other types of PH and PH with Eisenmenger syndrome, confirmed or suspected pulmonary veno-occlusive disease or pulmonary capillary hemangiomatosis.

Design outcomes

Primary

MeasureTime frame
Modified 4-strata risk assessment instrument;Risk changes from baseline to the first follow-up by modified 4-strata risk assessment instrument;

Secondary

MeasureTime frame
Kaplan–Meier curve;Risk classification by modified 4-strata risk assessment instrument;

Countries

China

Contacts

Public ContactZhihong Liu

Fuwai Hospital

zhihongliufuwai@163.com+86 10 6833 6038

Outcome results

None listed

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