Informações:
Falhas:
ID
39414
Descrição
Acute Optimization of Cardiac Resynchronization Therapy (CRT)Using Echocardiography and SonR; ODM derived from: https://clinicaltrials.gov/show/NCT01293526
Link
https://clinicaltrials.gov/show/NCT01293526
Palavras-chave
Versões (1)
- 09/01/2020 09/01/2020 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
9 de janeiro de 2020
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Heart Failure NCT01293526
Eligibility Heart Failure NCT01293526
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT01293526
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Indication Implantation of CRT-D
Item
must have been indicated for implantation or upgrade to a crt-d system in the last 3 months
boolean
C3146298 (UMLS CUI [1,1])
C1135480 (UMLS CUI [1,2])
C1135480 (UMLS CUI [1,2])
Indication CRT
Item
indicated for crt according to current guidelines
boolean
C3146298 (UMLS CUI [1,1])
C1167956 (UMLS CUI [1,2])
C1167956 (UMLS CUI [1,2])
QRS duration
Item
qrs duration between 120 ms and 150 ms
boolean
C0429025 (UMLS CUI [1])
Informed Consent
Item
able and willing to provide consent and authorization of use of phi
boolean
C0021430 (UMLS CUI [1])
Myocardial Infarction | Acute Coronary Syndrome
Item
myocardial infarction or acute coronary syndrome deemed inappropriate for trial per the investigator within 90 days of implant
boolean
C0027051 (UMLS CUI [1])
C0948089 (UMLS CUI [2])
C0948089 (UMLS CUI [2])
Cardiac Surgery Planned | Cardiac Surgery Recent | Revascularization Planned | Revascularization Recent
Item
planned, or recent heart surgery or revascularization within the last three months
boolean
C0018821 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0018821 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
C0581603 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0581603 (UMLS CUI [4,1])
C0332185 (UMLS CUI [4,2])
C1301732 (UMLS CUI [1,2])
C0018821 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
C0581603 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0581603 (UMLS CUI [4,1])
C0332185 (UMLS CUI [4,2])
Study Subject Participation Status | Clinical Trial
Item
already enrolled in other study that precludes enrollment in this study per principal investigator
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
C0008976 (UMLS CUI [2])
Pregnancy
Item
known pregnancy at the time of enrollment
boolean
C0032961 (UMLS CUI [1])
Age
Item
age less than 18 at the time of enrollment
boolean
C0001779 (UMLS CUI [1])
Compliance behavior Unable Follow-up
Item
unable to comply with follow-up requirements
boolean
C1321605 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Chronic atrial fibrillation
Item
chronic atrial fibrillation
boolean
C0694539 (UMLS CUI [1])
Compliance behavior Lacking
Item
recent history of medical non-compliance as determined by the investigator
boolean
C1321605 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide consent and authorization of use of phi
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])