Informações:
Falhas:
ID
16750
Descrição
Preliminary Study Examining Heart Failure Patients Responses to Depression Education; ODM derived from: https://clinicaltrials.gov/show/NCT01794598
Link
https://clinicaltrials.gov/show/NCT01794598
Palavras-chave
Versões (1)
- 03/08/2016 03/08/2016 -
Transferido a
3 de agosto de 2016
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Chronic Heart Failure NCT01794598
Eligibility Chronic Heart Failure NCT01794598
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Heart Failure NCT01794598
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
lvef
Item
lvef ≤ 35%.
boolean
C0428772 (UMLS CUI [1])
nyha
Item
nyha class ii, iii, or iv heart failure for the previous three months despite a minimum of 6 weeks of treatment.
boolean
C1275491 (UMLS CUI [1])
heart failure therapy, beta blockers
Item
must be on optimal heart failure therapy according to aha/acc and hfsa heart failure guidelines, including treatment with acei and beta-blocker therapy, or have documented rationale for variation, including intolerance, contraindication, patient preference, or personal physician's judgment.
boolean
C0087111 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0001645 (UMLS CUI [2])
C0018801 (UMLS CUI [1,2])
C0001645 (UMLS CUI [2])
age
Item
age less than 18.
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
currently pregnant or intending to become pregnant in the next year.
boolean
C0032961 (UMLS CUI [1])
cardiovascular procedure or hospitalization
Item
cardiovascular procedure or hospitalization for any reason planned in the next 6 months.
boolean
C0189573 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
C0019993 (UMLS CUI [2])
expected cardiac transplant
Item
expectation of receiving a cardiac transplant in the next six months.
boolean
C0018823 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,2])
study consent
Item
unable to provide the study consent.
boolean
C4034855 (UMLS CUI [1])
study participation
Item
participation another clinical trial(s) that may interfere with follow-up or data collection for this study, or that may affect cardiovascular mortality.
boolean
C2348568 (UMLS CUI [1])