Información:
Error:
ID
39477
Descripción
Integrated Diagnostic for Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT01798797
Link
https://clinicaltrials.gov/show/NCT01798797
Palabras clave
Versiones (1)
- 15/1/20 15/1/20 -
Titular de derechos de autor
See clinicaltrials.gov
Subido en
15 de enero de 2020
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Heart Failure NCT01798797
Eligibility Heart Failure NCT01798797
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT01798797
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Age
Item
patient is 18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Informed Consent | Informed Consent Patient Representative
Item
patient ( or patient's legally authorized representative) is willing and able to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Compliance behavior Follow-up visit
Item
patient is willing and able to comply with the required study follow up visits
boolean
C1321605 (UMLS CUI [1,1])
C0589121 (UMLS CUI [1,2])
C0589121 (UMLS CUI [1,2])
Implantable defibrillator insertion | Implantation of CRT-D | Other Coding
Item
patient is implanted with a medtronic wireless icd or crt-d device capable of optivol fluid monitoring feature
boolean
C0877213 (UMLS CUI [1])
C1135480 (UMLS CUI [2])
C3846158 (UMLS CUI [3])
C1135480 (UMLS CUI [2])
C3846158 (UMLS CUI [3])
Enrollment Network Specified
Item
patient is on medtronic carelink network or is willing to be enrolled on the carelink network
boolean
C1516879 (UMLS CUI [1,1])
C1882071 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C1882071 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Disease Management Heart failure Clinician
Item
patient is being managed, or has been managed, by a hf clinician
boolean
C0376636 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0871685 (UMLS CUI [1,3])
C0018801 (UMLS CUI [1,2])
C0871685 (UMLS CUI [1,3])
Informed Consent Network Specified
Item
patient has signed an informed consent for carelink network services
boolean
C0021430 (UMLS CUI [1,1])
C1882071 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C1882071 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Implanted device
Item
patient is implanted with device for at least three months
boolean
C0021102 (UMLS CUI [1])
Use of Monitor Specified | Data Transmission
Item
patient is willing and able to transmit data using the carelink home monitor (2490c).
boolean
C1524063 (UMLS CUI [1,1])
C0181904 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C0332289 (UMLS CUI [2])
C0181904 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C0332289 (UMLS CUI [2])
Study Subject Participation Status | Clinical Trial Interferes with Protocol Compliance
Item
patient is participating in another study that may interfere with triage-hf protocol required procedures
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
Cardiac implant device Problem
Item
patient with an implantable cardiac device that is indicated to reach eri in less than 12 months
boolean
C0581396 (UMLS CUI [1,1])
C0033213 (UMLS CUI [1,2])
C0033213 (UMLS CUI [1,2])