심부전-USB: 예측 및 진행 (HF-USB)
This retrospective cohort study is to identify triggers of heart failure (HF) development and drivers of HF progression as well as the underlying cardiac disease (phenotype) to identify patients at risk and predict the clinical course of the disease. Data of patients who were hospitalized during the years 2010-2023 with acute coronary syndrome (ACS) and/ or with acute heart failure (AHF) will be collected and analyzed. In a subgroup cohort efficacy and safety of digoxin in patients with acute heart failure triggered by tachyarrhythmia will be evaluated.
연구 개요
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Christian Müller, Prof. Dr.
- 전화번호: 0041 6132 86 549
- 이메일: Christian.mueller@usb.ch
연구 연락처 백업
- 이름: Fiona Nafaa, MD
- 전화번호: +41 61 32 87747
- 이메일: fiona.nafaa@usb.ch
연구 장소
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Basel, 스위스, 4031
- 모병
- Cardiology, University Hospital Basel
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연락하다:
- Christian Mueller, Prof. Dr.
- 전화번호: +41 61 32 86 549
- 이메일: Christian.mueller@usb.ch
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
Patients that were hospitalized at the Universitätsspital Basel/ Switzerland with the diagnosis of ACS or AHF during the years 2010 - 2023
설명
Inclusion Criteria:
- Patients hospitalized with a primary diagnosis of ACS
- Patients hospitalized with a primary or secondary diagnosis of AHF
Exclusion Criteria:
- Existence of a documented statement of the patient against the scientific use of clinical data
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 관찰 모델: COHORT
- 시간 관점: RETROSPECTIVE
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
acute coronary syndrome (ACS)
Outcome information (all-cause death, heart failure (HF) hospitalizations) of patients hospitalized with a primary diagnosis of ACS is analyzed. |
data generated by medical review include Medical history, Medications at presentation, during hospitalization and at discharge, New York Heart Association (NYHA) class, Killip class, Electrocardiographic (ECG) data, echocardiographic data, Interventions (Percutaneous Coronary Intervention (PCI), Coronary Artery Bypass Graft (CABG), Implantable Cardioverter Defibrillator (ICD) implantation, Cardiac Resynchronization Therapy (CRT) Implantation), Outcome Information: all-cause death, HF hospitalizations data generated by direct IT export include Anthropometric data (age, sex, height, weight), Vital signs, Laboratory data |
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acute heart failure (AHF)
Outcome information (all-cause death, heart failure (HF) hospitalizations) of patients hospitalized with a primary or secondary diagnosis of AHF is analyzed. |
data generated by medical review include Medical history, Medications at presentation, during hospitalization and at discharge, New York Heart Association (NYHA) class, Killip class, Electrocardiographic (ECG) data, echocardiographic data, Interventions (Percutaneous Coronary Intervention (PCI), Coronary Artery Bypass Graft (CABG), Implantable Cardioverter Defibrillator (ICD) implantation, Cardiac Resynchronization Therapy (CRT) Implantation), Outcome Information: all-cause death, HF hospitalizations data generated by direct IT export include Anthropometric data (age, sex, height, weight), Vital signs, Laboratory data |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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number of all-cause death
기간: 1 to 8 years after hospitalization
|
number of all-cause death in patients hospitalized with ACS and AHF during the years 2010-2023. |
1 to 8 years after hospitalization
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|
number of HF hospitalizations
기간: 1 to 8 years after hospitalization
|
number of new HF hospitalizations in patients hospitalized with ACS and AHF during the years 2010-2023 |
1 to 8 years after hospitalization
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|
number of cardiovascular death
기간: 1 to 8 years after hospitalization
|
number of cardiovascular death in patients hospitalized with ACS and AHF |
1 to 8 years after hospitalization
|
|
number of cardiovascular hospitalizations
기간: 1 to 8 years after hospitalization
|
number of cardiovascular hospitalizations |
1 to 8 years after hospitalization
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Christian Müller, Prof. Dr., Cardiology University Hospital Basel
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
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 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .