跳至主要内容
临床试验/NCT07001007
NCT07001007招募中不适用

SCAPIS 2 Cardio - Vibrometer Based Pulse Wave Analysis and CVD Risk Assessment

HJN Sverige AB/Neko Health1 个研究点 分布在 1 个国家目标入组 1,600 人开始时间: 2024年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,600
试验地点
1
主要终点
Area under receiver operating curve (ROC) to predict CAD-RADS ≥2

研究概览

简要总结

This clinical investigation will evaluate a novel contactless technology for assessing arterial stiffness and pulse wave characteristics and explore its potential in assessment of coronary artery disease, aortic stenosis and heart failure, in a population-based sample aged 58-72 years.

It will be the first in clinical setting, pilot stage, observational investigation to evaluate the clinical safety, performance and diagnostic accuracy of Cardio P4, a laser-doppler vibrometry (LDV) and microwave radar-based device.

详细描述

Cardiovascular disease (CVD) is the leading cause of death globally, placing a large burden on the healthcare system.

In asymptomatic individuals, there exists several risk scores to predict cardiovascular events (like SCORE2, SCORE2-OP and Framinham Risk Score). In patients with suspected symptoms of coronary artery disease, the European Society of Cardiology advice to estimate the pre-test probability by the risk factor-weighted clinical likelihood (RF-CL).

Most of these scores include the key factors for CAD development including age, sex, LDL- (or non-HDL) cholesterol, diabetes, smoking history, blood pressure or hypertension. Coronary computed tomography angiography (CCTA) is one of the main recommended examinations at low-intermediary risk based on PTP. While the procedure is non-invasive and relatively safe in comparison to invasive alternatives, they still represent a risk to the patient by radiation exposure and incidental findings, and is associated with lack of availability.

One key issue is that once a patient has a CCTA performed showing coronary atherosclerosis, that entails optimized prevention, with solid evidence. However, patients without symptoms of CAD are less studied regarding the degree of CAD. The present SCAPIS trial is the largest such trial on CCTA in 30 000 patients age 50 to 64 years, 25 182 individuals without known coronary heart disease were included. In these asymptomatic persons, CCTA-detected atherosclerosis was found in 42.1% and a significant stenosis (≥50%) in 5.2%.

Arterial stiffness, commonly assessed as pulse wave velocity (PWV), is a marker of aging of the cardiovascular system, and is independently associated with coronary artery disease. Increased arterial stiffness is an early indicator of cardiovascular disease and may improve precision in risk stratification. Laser-Doppler and microwave radar are new promising methods for analysis of pulse waves in human blood vessels. The technology may be more suitable for screening through enabling lower operator dependence and faster assessment time in comparison to standard assessment methods, and may contribute to lower overall healthcare costs and improved precision in identification of CVD.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
58 Years 至 72 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Subjects already included in the main / general SCAPIS 2 study at Danderyd Hospital in Stockholm, and of which has also participated in the echocardiography examination

排除标准

  • •Patients unable to provide an informed consent

结局指标

主要结局

Area under receiver operating curve (ROC) to predict CAD-RADS ≥2

时间窗: Typically within 2 months of enrolment

Change in area under receiver operating curve (ROC) to predict CAD-RADS ≥2 when adding Vibrometer-based SSN femoral PWV to the standard risk factors. Coronary artery disease reporting and data system (CAD-RADS) ≥2 refers to the classification of coronary artery disease with at least moderate stenosis as identified on coronary computer tomography angiography. The classification follows the CAD-RADS 2.0 definition. Stenosis is graded in severity from 0-5.

次要结局

  • Correlation between vibrometer-based PWA from the suprasternal notch and PWV by Arteriograph(Typically within 2 months of enrolment)
  • Area under receiver operating curve (ROC) to predict CAD-RADS ≥3(Typically within 2 months of enrolment)
  • Area under receiver operating curve (ROC) to predict CAD-RADS ≥2(Typically within 2 months of enrolment)
  • Area under receiver operating curve (ROC) to predict CAD-RADS ≥2 stratified by sex(Typically within 2 months of enrolment)
  • Area under receiver operating curve (ROC) to predict CAD-RADS ≥2 stratified by body mass index strata(Typically within 2 months of enrolment)
  • Correlation between vibrometer-based PWA from the suprasternal notch and CAD-RADS score(Typically within 2 months of enrolment)
  • Correlation between pressure sensor (piezo) based PWV and CAD-RADS score(Typically within 2 months of enrolment)
  • Correlation between vibrometer-based PWV and CAC score(Typically within 2 months of enrolment)
  • Machine learning analysis of Vibrometer signals(Same day as enrolment)
  • Correlation between vibrometer-based PWV and left ventricular mass index(Same day as enrolment)
  • Correlation between vibrometer-based left ventricular ejection time and left ventricular ejection fraction(Same day as enrolment)
  • Correlation between vibrometer-based PEP/LVET ratio and LVEF(Same day as enrolment)
  • Correlation between vibrometer-based LVET and degree of aortic stenosis(Same day as enrolment)
  • Correlation between vibrometer-based PEP/LVET ratio and degree of aortic stenosis(Same day as enrolment)
  • Correlation between vibrometer-based LVET and degree of aortic valve calcification(Same day as enrolment)
  • Correlation between vibrometer-based PEP/LVET and degree of aortic valve calcification(Same day as enrolment)
  • Correlation between vibrometer-based LVET and markers of diastolic dysfunction(Same day as enrolment)
  • Correlation between vibrometer-based PEP/LVET markers of diastolic dysfunction(Same day as enrolment)

研究者

发起方
HJN Sverige AB/Neko Health
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验