ID

44467

Description

Atorvastatin Plus Ezetimibe on Coronary Plaque Progression; ODM derived from: https://clinicaltrials.gov/show/NCT01086020

Link

https://clinicaltrials.gov/show/NCT01086020

Keywords

  1. 12/14/18 12/14/18 -
  2. 9/27/21 9/27/21 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 27, 2021

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01086020

Eligibility Coronary Artery Disease NCT01086020

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
willing to receive the coronary angiography and potential pci therapy
Description

Coronary angiography Willing | Percutaneous Coronary Intervention potential Willing

Data type

boolean

Alias
UMLS CUI [1,1]
C0085532
UMLS CUI [1,2]
C0600109
UMLS CUI [2,1]
C1532338
UMLS CUI [2,2]
C3245505
UMLS CUI [2,3]
C0600109
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients was treated by statins before randomization
Description

Statins

Data type

boolean

Alias
UMLS CUI [1]
C0360714
patient with ≤ 20% and ≥ 70% coronary narrowing and target lesion
Description

Coronary Stenosis Percentage | Target Lesion

Data type

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C0439165
UMLS CUI [2]
C2986546
st elevation myocardial infarction less than 7 days
Description

ST elevation myocardial infarction Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C1536220
UMLS CUI [1,2]
C0449238
without informed consent
Description

Informed Consent Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
abnormal liver function before randomization, (ast, alt ≥uln)
Description

Liver Dysfunction | Aspartate aminotransferase measurement | Alanine aminotransferase measurement

Data type

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201836
active hepatitis or muscular disease
Description

Hepatitis | Myopathy

Data type

boolean

Alias
UMLS CUI [1]
C0019158
UMLS CUI [2]
C0026848
impaired renal function with serum creatinine level > 3mg/dl
Description

Renal Insufficiency | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0201976
impaired left ventricular function with lvef > 30%
Description

Impaired left ventricular function | Left ventricular ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0242698
UMLS CUI [2]
C0428772
participate in other studies
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Coronary Artery Disease NCT01086020

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Coronary angiography Willing | Percutaneous Coronary Intervention potential Willing
Item
willing to receive the coronary angiography and potential pci therapy
boolean
C0085532 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C3245505 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Statins
Item
patients was treated by statins before randomization
boolean
C0360714 (UMLS CUI [1])
Coronary Stenosis Percentage | Target Lesion
Item
patient with ≤ 20% and ≥ 70% coronary narrowing and target lesion
boolean
C0242231 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C2986546 (UMLS CUI [2])
ST elevation myocardial infarction Duration
Item
st elevation myocardial infarction less than 7 days
boolean
C1536220 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Informed Consent Lacking
Item
without informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Liver Dysfunction | Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
abnormal liver function before randomization, (ast, alt ≥uln)
boolean
C0086565 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
Hepatitis | Myopathy
Item
active hepatitis or muscular disease
boolean
C0019158 (UMLS CUI [1])
C0026848 (UMLS CUI [2])
Renal Insufficiency | Creatinine measurement, serum
Item
impaired renal function with serum creatinine level > 3mg/dl
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Impaired left ventricular function | Left ventricular ejection fraction
Item
impaired left ventricular function with lvef > 30%
boolean
C0242698 (UMLS CUI [1])
C0428772 (UMLS CUI [2])
Study Subject Participation Status
Item
participate in other studies
boolean
C2348568 (UMLS CUI [1])

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