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coMparison Between invAsive and Non-invasive assessmenT on Blood Pressure and Cardiac Function in HealthY Participants (MATCHY)

T

Tongji University

Status

Unknown

Conditions

Healthy Volunteer

Treatments

Diagnostic Test: Invasive left ventricular diastolic function assessment
Diagnostic Test: Non-Invasive left ventricular diastolic function assessment
Diagnostic Test: Non-Invasive aortic blood pressure measurement
Diagnostic Test: Invasive aortic blood pressure measurement

Study type

Observational

Funder types

Other

Identifiers

NCT03372616
MATCHY2017YZ

Details and patient eligibility

About

This is a cross-sectional cohort study which aims to compare the invasive and non-invasive assessments on aortic blood pressure and cardiac funtion in subjects without history of cardio-vascular disease. Left ventricular (LV) filling pressure, LV volume, and aortic blood pressure will be measured invasively. Non-invasive assessment includes echocardiography,aortic, and carotid blood pressure measurement.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over or equal to 18 years old;
  • Agree to participate the study and sign informed written consent;
  • Any change of drugs which effect the hemodynamics during 1 month prior to enrollment;
  • Proposed to perform coronary angiography and left left ventriculography in hospital;

Exclusion criteria

  • Non-sinus rhythm or frequent extra systoles;
  • Identified coronary artery disease via coronary angiography;
  • Diagnosed pulmonary vascular or parenchymal disease;
  • Hypertrophic cardiomyopathy, restrictive cardiomyopathy, or constrictive pericarditis;
  • Stenosis or insufficiency of valves (moderate and above);
  • Heart transplant;
  • Congenital heart disease;
  • Inadequate imaging or doppler parameter quality in echocardiography.

Trial design

100 participants in 1 patient group

All participants
Description:
Aortic blood pressure, LV filling pressrue, and LV volume will be measured in all participants. Meanwhile, echocardiography and non-invasive aortic blood presure measurement will be performed. Three devices will be used in non-invasive aortic blood presure measurement, including Sphygmocor (AtCor Medical, Australia), PulsePen (DiaTecne SRL, Italy), and Mobil-O-Graph (IEM, Germany). In conclusion, all participants will receive invasive and non-invasive left ventricular diastolic function assessment, together with invasive and non-invasive aortic blood pressure assessment.
Treatment:
Diagnostic Test: Invasive aortic blood pressure measurement
Diagnostic Test: Non-Invasive aortic blood pressure measurement
Diagnostic Test: Non-Invasive left ventricular diastolic function assessment
Diagnostic Test: Invasive left ventricular diastolic function assessment

Trial contacts and locations

0

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Central trial contact

Yi Zhang, M.D., Ph.D.; Chen Chi, M.D.

Data sourced from clinicaltrials.gov

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