ClinicalTrials.Veeva

Menu

Multi-marker Approach for Risk Assessment in PAH (MARS)

W

Wuhan Asia Heart Hospital

Status

Enrolling

Conditions

Pulmonary Arterial Hypertension

Study type

Observational

Funder types

Other

Identifiers

NCT03954405
2018LMC-1

Details and patient eligibility

About

Prospective registry including incident patients and prevalent patients which pretends to identify clinical characteristics, treatment trends in-hospital and ten years follow-up outcome through major adverse cardiovascular events (MACE) in a China population with well characterized PAH.

Full description

baseline include: An echocardiogram to assess the size, shape, pumping action and the extent of any damage to the heart.

Lung function tests which include blowing measurements to assess gas volumes within the lungs as well as assessment of how the lungs exchange gases.

Right heart catheterisation (RHC) to diagnose PAH Optional Cardiac Magnetic Resonance tests. 6 minute walk distance (6MWD). To measure exercise capacity Electrocardiogram (ECG), a test that measures the electrical activity of the heart Blood tests

MACE include:

death heart/lung transplantation atrial septostomy hospitalization due to worsening of PAH start of new specific PAH treatment persistent decrease of >15% from baseline in 6MWD (or >30% compared with last study-related measurement) persistent worsening of World Health Organization (WHO) Functional Class (FC)

Enrollment

500 estimated patients

Sex

All

Ages

1 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

diagnosis of PAH (by RHC)

Exclusion criteria

Refusal to participate.

Trial contacts and locations

1

Loading...

Central trial contact

Zheng Xusn

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems