Determination of Specificity and Sensitivity in Detecting Myocardial Infarction Using the EDE CARDIO BIO-MAP Machine (CARDIO BIO-MAP)
Determination of Specificity and Sensitivity in Detecting Myocardial Infarction Using the EDE CARDIO BIO-MAP Machine, the EDE CARDIO BIO-MAP Study
The goal of this observational study is to learn whether a non-invasive electromagnetic wave scanner (EDE CARDIO BIO-MAP) can help diagnose myocardial infarction (heart attack) in adults (18 years and older) who come to the emergency department with chest pain and suspected myocardial infarction. The main questions it aims to answer are:
- How sensitive and specific is the EDE scanner in diagnosing myocardial infarction (MI) compared with standard blood tests (e.g., cardiac troponin)?
- How sensitive and specific are the immediate blood measurements from a portable lab device compared with conventional hospital laboratory measurements? Researchers will compare the results of the EDE scanner and the portable lab with standard hospital blood test results and the final clinical diagnosis to see how accurately each detects MI.
Participants will:
- Have a research visit (30 minutes to 1 hour) during their emergency care, including a quick scan with the Exponential Deep Examination (EDE) device (attached to a phone or tablet) and a small research blood sample tested on a portable lab device
- Repeat the scan and blood sample 4 to 6 hours later, only if a second blood draw is already needed for their clinical care
- Answer questions about their medical and social history, and allow the study team to collect relevant results from their medical record Scanner results will not be shared with participants or used for their clinical care.
연구 개요
상태
상태
정황
정황
상세 설명
Myocardial infarction is a leading cause of death and disability worldwide. Current diagnosis relies on clinical assessment, electrocardiogram, and blood measurement of cardiac biomarkers such as troponin. Faster, non-invasive diagnostic tools could be especially valuable in the emergency setting, where timely intervention is critical.
The Exponential Deep Examination Cardio Bio-Map is a non-invasive device, classified as Class 1 under the European Conformity marking system, that analyzes passive electromagnetic signals (0.1 to 300 gigahertz) using artificial intelligence to measure cardiac biomarkers without a blood draw. Results are available within 50 milliseconds. The device does not collect or store patient data. It produces an immediate printed report, and all data processing occurs locally within Qatar. During the COVID-19 pandemic, the same technology detected the SARS-CoV-2 virus with a specificity of 95.62% and a sensitivity of 93.71% compared with polymerase chain reaction testing and antibody testing. This study will evaluate whether the device can screen for myocardial infarction through measurement of cardiac biomarkers, both in biological samples (in vitro, using a portable laboratory device) and directly in patients (in vivo, using the scanner).
연구 유형
연구 유형
등록 (추정된)
등록
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Charbel Abi Khalil, MD,PhD
- 전화번호: +974 4492 8484
- 이메일: cha2022@qatar-med.cornell.edu
참여기준
자격 기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
Participants will be recruited at Hamad Medical Corporation
설명
Inclusion Criteria:
- Age ≥18 years.
- Adults presenting to the emergency room for acute chest pain.
- English or Arabic speakers.
Exclusion Criteria:
- Pregnancy (self-reported).
- Adults with cognitive disorders.
- Unconscious patients.
- Citizens from countries where the General Data Protection Regulation (GDPR) applies, due to regulatory constraints.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 관찰 모델: COHORT
- 시간 관점: PROSPECTIVE
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Sensitivity and specificity of the EDE CARDIO BIO-MAP scanner(in vivo) for detecting myocardial infarction
기간: Baseline
|
Sensitivity (true positives / [true positives + false negatives]) and specificity (true negatives / [true negatives + false positives]) of the scanner in emergency room patients with suspected myocardial infarction, compared with standard hospital laboratory results (cardiac troponin, creatine kinase-myocardial band, myoglobin, B-type natriuretic peptide, N-terminal pro-B-type natriuretic peptide) and the final clinical diagnosis in the medical record. |
Baseline
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Sensitivity and specificity of the portable lab's immediate blood measurements (in vitro)
기간: Baseline
|
Sensitivity and specificity of the portable lab's immediate blood measurements for myocardial infarction, compared with conventional hospital laboratory measurements, using a confusion matrix. |
Baseline
|
|
Accuracy of the EDE scanner
기간: Baseline
|
Accuracy = (true positives + true negatives) / all results; |
Baseline
|
|
Misclassification rate of the EDE scanner
기간: Baseline
|
Misclassification rate = (false positives + false negatives) / all results; |
Baseline
|
|
Precision of the EDE scanner
기간: Baseline
|
precision = true positives / (true positives + false positives) |
Baseline
|
|
Accuracy of the portable lab
기간: Baseline
|
Accuracy = (true positives + true negatives) / all results; |
Baseline
|
|
Misclassification rate of the portable lab
기간: Baseline
|
Misclassification rate = (false positives + false negatives) / all results; |
Baseline
|
|
Precision of the portable lab
기간: Baseline
|
precision = true positives / (true positives + false positives) |
Baseline
|
|
Correlation Between EDE Scanner and Portable Laboratory Values for Cardiac Biomarkers
기간: Baseline
|
Pearson or Spearman correlation coefficient between scanner and portable lab values for cardiac biomarkers : Troponin T, Troponin I, Myoglobin, B-type Natriuretic Peptide, NT-proBNP, and Creatine Kinase-MB. |
Baseline
|
|
Predictive power of each cardiac biomarker for myocardial infarction
기간: Baseline
|
Logistic regression, area under the receiver operating characteristic curve, and optimal diagnostic cutoffs for each cardiac biomarker: Troponin T, Troponin I, Myoglobin, B-type Natriuretic Peptide, NT-proBNP, and Creatine Kinase-MB. |
Baseline
|
기타 결과 측정
기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in cardiac biomarker levels between initial assessment and 4-6 hour follow-up
기간: Baseline and 4-6 hours after initial assessment
|
Change in cardiac biomarker levels( Troponin T, Troponin I, Myoglobin, B-type Natriuretic Peptide, NT-proBNP, and Creatine Kinase-MB) between the initial assessment and the follow-up, in participants who have a second clinical blood draw. |
Baseline and 4-6 hours after initial assessment
|
|
Diagnostic performance of the scanner by sex
기간: Baseline
|
Subgroup analysis of scanner sensitivity and specificity by sex |
Baseline
|
|
Diagnostic performance of the scanner by age group
기간: Baseline
|
Subgroup analysis of scanner sensitivity and specificity by age group |
Baseline
|
|
Diagnostic performance of the scanner by symptom profile
기간: Baseline
|
Subgroup analysis of scanner sensitivity and specificity by symptom profile. |
Baseline
|
공동 작업자 및 조사자
협력자
협력자
수사관
수사관
- 수석 연구원: Charbel Abi Khalil, MD,PhD, Weill Cornell Medicine-Qatar
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- 23-00017
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
ongoing discussion with the sponsor
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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