ID

34263

Descrizione

Promoting Adherence to Improve Effectiveness of Cardiovascular Disease Therapies; ODM derived from: https://clinicaltrials.gov/show/NCT01251757

collegamento

https://clinicaltrials.gov/show/NCT01251757

Keywords

  1. 16/01/19 16/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

16 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus NCT01251757

Eligibility Diabetes Mellitus NCT01251757

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 40-80 years as of time of randomization.
Descrizione

ID.1

Tipo di dati

boolean

two or more medication dispensings for any prescription medication from a kp outpatient pharmacy during the baseline year.
Descrizione

ID.2

Tipo di dati

boolean

flagged in kp's databases as having either diabetes or atherosclerotic cardiovascular disease(defined as coronary artery disease, peripheral vascular disease, or a history of atherosclerotic stroke)
Descrizione

ID.3

Tipo di dati

boolean

continuous membership in kp for the 12 months prior to randomization.
Descrizione

ID.4

Tipo di dati

boolean

willing to participate in the study.
Descrizione

ID.5

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
evidence in the emr of allergy or intolerance to statins, ace inhibitors/arbs,or aspirin
Descrizione

ID.6

Tipo di dati

boolean

use of warfarin or other antiplatelet agents for which aspirin use is contraindicated
Descrizione

ID.7

Tipo di dati

boolean

end-stage renal disease or other conditions for which ace inhibitor or arb use is contraindicated
Descrizione

ID.8

Tipo di dati

boolean

use of medications for which use of statins is contraindicated
Descrizione

ID.9

Tipo di dati

boolean

Similar models

Eligibility Diabetes Mellitus NCT01251757

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
aged 40-80 years as of time of randomization.
boolean
ID.2
Item
two or more medication dispensings for any prescription medication from a kp outpatient pharmacy during the baseline year.
boolean
ID.3
Item
flagged in kp's databases as having either diabetes or atherosclerotic cardiovascular disease(defined as coronary artery disease, peripheral vascular disease, or a history of atherosclerotic stroke)
boolean
ID.4
Item
continuous membership in kp for the 12 months prior to randomization.
boolean
ID.5
Item
willing to participate in the study.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
evidence in the emr of allergy or intolerance to statins, ace inhibitors/arbs,or aspirin
boolean
ID.7
Item
use of warfarin or other antiplatelet agents for which aspirin use is contraindicated
boolean
ID.8
Item
end-stage renal disease or other conditions for which ace inhibitor or arb use is contraindicated
boolean
ID.9
Item
use of medications for which use of statins is contraindicated
boolean

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