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Informações:
Falhas:
ID
32508
Descrição
DECIDE-HF: Heart Rate Variability in Heart Failure Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00949676
Link
https://clinicaltrials.gov/show/NCT00949676
Palavras-chave
Versões (2)
- 05/11/2018 05/11/2018 -
- 20/09/2021 20/09/2021 -
Titular dos direitos
See clinicaltials.gov
Transferido a
5 de novembro de 2018
DOI
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Licença
Creative Commons BY-NC 3.0
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Eligibility Systolic Heart Failure NCT00949676
Eligibility Systolic Heart Failure NCT00949676
- StudyEvent: Eligibility
Similar models
Eligibility Systolic Heart Failure NCT00949676
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Informed Consent
Item
subject has signed and dated the study-specific informed consent form
boolean
C0021430 (UMLS CUI [1])
Age
Item
subject is 18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Study Subject Available Follow-up
Item
subject is expected to remain available for follow-ups
boolean
C0681850 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Protocol Compliance
Item
subject is able and willing to comply with the protocol requirements
boolean
C0525058 (UMLS CUI [1])
Normal sinus rhythm Predominant
Item
subject has predominant normal sinus rhythm
boolean
C0232202 (UMLS CUI [1,1])
C1542147 (UMLS CUI [1,2])
C1542147 (UMLS CUI [1,2])
Systolic Heart Failure New York Heart Association Classification | Cardiac ejection fraction
Item
subject has systolic heart failure and is at the moment of enrollment in nyha class ii or iii and has an ejection fraction of less then 40%
boolean
C1135191 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C0232174 (UMLS CUI [2])
C1275491 (UMLS CUI [1,2])
C0232174 (UMLS CUI [2])
Hospitalization Due to Heart Failure
Item
subject has had a hf-related hospitalization in the past 12 months
boolean
C3898876 (UMLS CUI [1])
Patient need for Intra-atrial pacing Permanent Percentage
Item
subject needs permanent atrial pacing (> 10%)
boolean
C0686904 (UMLS CUI [1,1])
C0199647 (UMLS CUI [1,2])
C0205355 (UMLS CUI [1,3])
C0439165 (UMLS CUI [1,4])
C0199647 (UMLS CUI [1,2])
C0205355 (UMLS CUI [1,3])
C0439165 (UMLS CUI [1,4])
Intermittent second degree atrioventricular block | Complete atrioventricular block Intermittent
Item
subject has intermittent 2nd or intermittent 3rd degree block
boolean
C0344418 (UMLS CUI [1])
C0151517 (UMLS CUI [2,1])
C0205267 (UMLS CUI [2,2])
C0151517 (UMLS CUI [2,1])
C0205267 (UMLS CUI [2,2])
Persistent atrial fibrillation | Permanent atrial fibrillation
Item
subject has persistent or permanent af
boolean
C2585653 (UMLS CUI [1])
C2586056 (UMLS CUI [2])
C2586056 (UMLS CUI [2])
Long QT Syndrome | Brugada Syndrome | Jervell-Lange Nielsen Syndrome | Romano-Ward Syndrome | Andersen Tawil Syndrome | Timothy syndrome
Item
subject has long qt syndrome, brugada syndrome, jervell and lange- nielsen syndrome, romano-ward syndrome, andersen-tawil syndrome or timothy's syndrome
boolean
C0023976 (UMLS CUI [1])
C1142166 (UMLS CUI [2])
C0022387 (UMLS CUI [3])
C0035828 (UMLS CUI [4])
C1563715 (UMLS CUI [5])
C1832916 (UMLS CUI [6])
C1142166 (UMLS CUI [2])
C0022387 (UMLS CUI [3])
C0035828 (UMLS CUI [4])
C1563715 (UMLS CUI [5])
C1832916 (UMLS CUI [6])
Acute Coronary Syndrome
Item
subject has had recent (<2 months) acute coronary syndrome
boolean
C0948089 (UMLS CUI [1])
Revascularization
Item
subject has had recent (<2 months) revascularization
boolean
C0581603 (UMLS CUI [1])
Heart Transplantation pending | Cardiac Revascularization pending
Item
subject has a pending cardiac transplant or revascularization
boolean
C0018823 (UMLS CUI [1,1])
C1611271 (UMLS CUI [1,2])
C0027056 (UMLS CUI [2,1])
C1611271 (UMLS CUI [2,2])
C1611271 (UMLS CUI [1,2])
C0027056 (UMLS CUI [2,1])
C1611271 (UMLS CUI [2,2])
Heart valve stenosis Severe
Item
subject has severe stenotic valvular heart disease
boolean
C0264878 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Lung disease Severe | FEV1 | Liver disease Severe | Kidney Disease Severe | Plasma creatinine measurement
Item
subject has severe pulmonary (forced expiratory volume in 1 s < 1 l) hepatic or renal (plasma creatinine > 0.2 mmol/l) disease
boolean
C0024115 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0849974 (UMLS CUI [2])
C0023895 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0022658 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C1278055 (UMLS CUI [5])
C0205082 (UMLS CUI [1,2])
C0849974 (UMLS CUI [2])
C0023895 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0022658 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C1278055 (UMLS CUI [5])
Study Subject Participation Status Affecting Research results
Item
subject is participating in another study that may affect the results of this study
boolean
C2348568 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C0392760 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])