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临床试验/NCT03227848
NCT03227848已完成不适用

eMurmur ID - Clinical Performance Evaluation

CSD Labs GmbH1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2017年1月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
CSD Labs GmbH
入组人数
120
试验地点
1
主要终点
eMurmur ID sensitivity and specificity

研究概览

简要总结

The differentiation between innocent and pathologic murmurs through traditional auscultation can often be challenging, which in the end makes the diagnosis strongly dependent on the clinitians experience and clinical expertise. With the development of technology it is now possible to help diagnose heart murmurs using computer aided auscultation systems (CAA). eMurmur ID is an investigational CAA system (not FDA cleared) and the investigators hypothesize that it can distinguish between AHA class I (pathologic murmurs) and AHA class III heart sounds (innocent murmurs and/or no murmurs) with a sensitivity and specificity not worse compared to a similar FDA cleared CAA system on market.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
1 Day 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All age groups of patients will be included from 1day old
  • Patients who are being followed for known congenital heart disease and are returning for follow up
  • Patients referred for a suspected heart murmur

排除标准

  • Mismatch between the expert physician's diagnosis (auscultation based) and the diagnosis resulting from echocardiography (independently read by a cardiologist blinded to the auscultation results). Note: both, the expert physician and echocardiography results must independently reach the same diagnosis, which is then accepted as the gold standard reference diagnosis to which both devices are compared to. This is necessary because not every pathology visible on an echocardiogram causes an audible murmur, and not every murmur heard by a medical expert might correlate to pathology.
  • Patient whose behaviour does not allow for a standard auscultation by the physician (e.g. a screaming fit).

结局指标

主要结局

eMurmur ID sensitivity and specificity

时间窗: 1 day

The primary endpoints of the study are sensitivity and specificity. The clinical reference gold standard diagnosis is defined as expert physicians' diagnosis confirmed by independently interpreted echocardiogram diagnosis. True positive (TP), true negative (TN), false positive (FP) and false negative (FN) will be determined via comparison of the heart murmur classification results with the clinical gold standard (echocardiogram) diagnosis.

次要结局

未报告次要终点

研究者

发起方
CSD Labs GmbH
申办方类型
Other
责任方
Sponsor

研究点 (1)

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