跳至主要内容
临床试验/NCT06139094
NCT06139094已完成不适用

Magnetocardiography as a Noninvasive Diagnostic Strategy for Suspected Myocardial Ischemia With the Absence of Obstructive Coronary Artery Disease As Confirmed by Thermodilution-Derived CFR

Genetesis Inc.4 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2023年12月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
48
试验地点
4
主要终点
Detection of Myocardial Ischemia in the Absence of Obstructive Coronary Artery Disease (INOCA)

研究概览

简要总结

This study will be an observational registry to investigate the ability of magnetocardiography (MCG) in determining the presence of myocardial ischemia with the absence of obstructive coronary artery disease, by using an invasive reference standard coronary flow reserve (CFR) measured using thermodilution for diagnosis. The device is a magnetocardiography (MCG) scanner named CardioFlux, which is paired with cloud processing software. A CardioFlux scan appointment shall last approximately 15 minutes in duration and include a patient questionnaire following the scan.

详细描述

This observational registry study focuses on investigating the efficacy of magnetocardiography (MCG) in detecting myocardial ischemia secondary to coronary microvascular dysfunction (CMD) in the absence of obstructive coronary artery disease. The reference standard for diagnosis will be invasive coronary flow reserve (CFR) measured using thermodilution.

The study utilizes a magnetocardiography (MCG) scanner known as CardioFlux, complemented by cloud processing software. The scanning procedure is designed to last approximately 15 minutes per participant, encompassing 5 minutes for patient preparation, 5 minutes for the CardioFlux scan, and an additional 5 minutes for a post-scan patient survey.

The primary objective is to assess the ability of MCG, through CardioFlux, to accurately determine the presence of myocardial ischemia in comparison to the reference standard CFR. The study will provide valuable insights into the diagnostic potential of MCG and its role in CMD detection, contributing to advancements in non-invasive cardiovascular diagnostics.

The primary study outcome measures shall be the detection of myocardial ischemia with no obstructive coronary artery disease (INOCA) using MCG-CF compared to Cardiac Thermodilution derived CFR. The secondary study outcome measures shall be the MCG Questionnaire, Demographic data (age, sex, height, weight, etc.), Relevant patient medical history, EKG results (if available), and Invasive CFR/angiogram results.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ≥ 18 years of age at the time of enrollment.
  • Signs and symptoms of coronary ischemia that prompted further evaluation by either invasive coronary angiography or coronary CT angiogram) within the previous 5 years.
  • Willing to provide written informed consent.
  • Non-obstructive CAD defined as: 0 to 49% diameter reduction of a major epicardial vessel or FFR>0.80 (or non-hyperemic equivalent of iFR or RFR >0.89)
  • Completed invasive CFR via thermodilution method within 6 months of informed consent.
  • Successfully passing CardioFlux's MCG ""Quality Preview" prior to MCG study scan.

排除标准

  • Patients unable to fit into the CardioFlux device.
  • Patients who meet device contraindications (as specified in section 1.4 of the protocol) NOTE: Sternotomy wires and stents are typically acceptable.
  • Patients unable to lie supine for 5 minutes.
  • History of non-ischemic dilated or hypertrophic cardiomyopathy.
  • Documented acute coronary syndrome (ACS) within the previous 30 days.
  • Known left ventricular ejection fraction (LVEF) <45%, or hospitalization for Reduced ejection fraction within 180 days. (HFpEF is permitted).
  • Currently in atrial fibrillation or atrial flutter at the time of enrollment.
  • Estimated glomerular filtration rate (eGFR) <30 ml/min.
  • Moderate or severe valvular disease (including aortic stenosis or insufficiency).
  • Life expectancy <1-yrs. due to non-cardiovascular comorbidity.
  • Concurrent enrollment in a clinical trial in which therapeutic intervention is administered within 30 days of enrollment.
  • Pregnancy.
  • Dextrocardia.
  • History of Left or Right Bundle Branch Block within 6 months of enrollment.

结局指标

主要结局

Detection of Myocardial Ischemia in the Absence of Obstructive Coronary Artery Disease (INOCA)

时间窗: 6 months

This observational registry study focuses on investigating the efficacy of magnetocardiography (MCG) in detecting myocardial ischemia secondary to coronary microvascular dysfunction (CMD) in the absence of obstructive coronary artery disease.

次要结局

  • Patient-Reported Experiences with MCG(6 months)
  • Invasive Coronary Flow Reserve (CFR) and Angiogram Outcomes(6 months)
  • Electrocardiogram (EKG)(6 months)
  • Participant Demographic Characteristics(6 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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