Feasibility and Functionality Test of Ada's DDSS Prototype (Ada4dyspnoe)
Feasibility and Functionality Test of Ada's DDSS Prototype, Exploring the Potential and Performance When Diagnosing Complex Cases of Dyspnea at the Emergency Department and Ward of Interna! Medicine of the University Hospital Basel
연구 개요
상세 설명
This is an observational i.e. non-interventional, prospective feasibility study, which assesses, through observation, the potential, functionality and diagnostic performance of the Ada DDSS prototype in evaluating patients presenting with dyspnea as primary predominant complaint to the ED.
Once the consent form is signed, the Investigator documents patients' data, medical history, symptoms and findings with the Ada DDSS prototype. During the entire patient journey through the hospital (presentation at the ED through to admission in the ward of Internal Medicine) relevant information are collected and documented in the Ada DDSS prototype simultaneously to standard documentation by the medical staff.
Examination and treatment are carried out by the attending physician without being influenced or affected by the entry of data in the Ada DDSS prototype.
There is no intervention/change made to the usual care, and therefore neither an intervention patient group nor a control patient group. The "usual care" that each patient receives is the control comparison point for the performance of the Ada DDSS. The diagnoses proposed by the tool at different times (after triage in the emergency centre, when transferred to the ward and when discharged from the hospital) are then compared with those of the attending physician.
연구 유형
등록 (실제)
연락처 및 위치
연구 장소
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Basel, 스위스, 4031
- University Hospital Basel
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Dyspnea as the main symptom when entering the emergency room
- Existence of written consent
- The patient is able to speak, understand and read German or English.
Exclusion Criteria:
- Inability or unwillingness to understand and comply with study procedures due to:
- Language problems
- Acute mental disorders
- Dementia
- Clinical instability (e..B. resuscitation treatment, non-invasive ventilation, etc.)
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Feasibility of the Ada DDSS prototype
기간: during hospital stay (presentation at the ED through to admission in the ward of Internal Medicine, in the average 1 week)
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Feasibility of the Ada DDSS prototype simultaneously to standard documentation by the medical staff.
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during hospital stay (presentation at the ED through to admission in the ward of Internal Medicine, in the average 1 week)
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Subjectively perceived benefit from using the Ada DDSS prototype
기간: during hospital stay (presentation at the ED through to admission in the ward of Internal Medicine, in the average 1 week)
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Subjectively perceived benefit from using the Ada DDSS prototype (during patient journey in the hospital) assessed by a physician.
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during hospital stay (presentation at the ED through to admission in the ward of Internal Medicine, in the average 1 week)
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공동 작업자 및 조사자
협력자
수사관
- 수석 연구원: Jens Eckstein, Prof. Dr. med., University Hospital, Basel, Switzerland
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
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
- 2020-00095; me19Eckstein3
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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