- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04910191
Collecting Respiratory Sound Samples From Corona Patients to Extend the Diagnostic Capability of VOQX Electronic Stethoscope to Diagnose COVID-19 Patients
Technological developments in the recent decades has enabled the integration of electronic and digital components in the stethoscope design, in an attempt to improve auditory performance and, moreover, to assist in improving user's diagnostic accuracy by incorporating computerized, digital technologies, artificial intelligence capabilities and deep-learning-based algorithms enhancing these devices.
We believe that these technologies can be used to significantly improve the diagnostic performance in the primary care phase, by means of a sophisticated stethoscope that enables auscultation to sounds and signals typically found in the sub-sound frequency level. Their transformation into the sound range, and the use of artificial intelligence and machine learning techniques to characterize sound patterns that correspond to specific problems or diseases can substantially enhance the physician's or other care giver's performance to the benefit of the patients.
At this stage, the software in development does not purport to make diagnostic decisions, but only to provide information that will enhance decision and diagnosis making process, therefore enable a more accurate and definitive diagnostic decision and perhaps decrease the number of additional diagnostic tests requested.
연구 개요
상세 설명
Up to 200 patients will participate in an open, prospective and multi-center study.
Patients diagnosed as positive to COVID-19 will be referred to a VOQX examination. All patients will receive detailed explanation about the purpose of the examination, its impact and will provide their consent prior to the examination. The VOQX device output will have no influence on the decision-making process of the physicians and care givers. The VOQX Stethoscope membrane will be put on the patient's chest area in predefined anterior and posterior points. The data collected in the form of breath sound signals in particular infra-sound will be transferred to an external computer and processed by machine learning algorithm developed by the company. The algorithm will seek patterns typical for the diagnosed disease for each corresponding case diagnosed.
연구 유형
등록 (예상)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Hadas Sapir
- 전화번호: 972 54 7826543
- 이메일: shadas@gsap.co.il
연구 장소
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Ashkelon, 이스라엘, 7830604
- 모병
- Barzilai Medical Center
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Hadera, 이스라엘, 38100
- 모병
- Hille Yaffe Medical Center
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Zrifin, 이스라엘, 703000
- 모병
- Shamir Medical Center (Assaf Harofah)
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Patients over the age of 18 years
- RT-PCR positive for COVID 19
Patients diagnosed with the following pulmonary pathology:
- Pneumonia
- Pulmonary edema
- Bronchitis
- Acute asthmatic attack
- Emphysema
- Or Normal (e.g. asymptomatic patients)
The diagnosis is confirmed if possible, by:
- Anamnesis
- Physical examination
- X-ray
- Suggestive blood test - CBC
- Pulse oximetry
Exclusion Criteria:
- Pregnant women
- Chest malformation
- Unconsciousness
- Subject that need a guardian
- Weigh above 150 Kg.
- Patients with current shortness of breath
- Patients currently assisted by breathing machine such as CPAP or other
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 상영
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Open Label
Up to 200 patients will participate in this open study. Before each examination with the study device, data from each patient (Current medical condition, medical history and demographic data) will be inserted to a computer and added to the database of the study for further processing in conjunction with the study device results. The study device electronic stethoscope membrane will be put on the patient's chest area in predefined anterior and posterior points. At the end of each examination the data will be transferred to a computer and stored in the patient's file. Each patient will be requested to attend the examination once. |
Electronic stethoscope
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Performance outcome
기간: Through study completion, an average of 1 year
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Detection and identification of pulmonary sound signals ranging from infra-sound to auditory sound which are typical to specific pathologies of COVID-19
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Through study completion, an average of 1 year
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Performance outcome
기간: through study completion, an average of 1 year
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Use machine learning technologies to identify the above sound patterns and corresponding pathologies
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through study completion, an average of 1 year
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공동 작업자 및 조사자
스폰서
수사관
- 연구 책임자: David Linhard, Sanolla
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- VOQX
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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