ID

39904

Description

Plaque REgression With Cholesterol Absorption Inhibitor or Synthesis Inhibitor Evaluated by IntraVascular UltraSound; ODM derived from: https://clinicaltrials.gov/show/NCT01043380

Link

https://clinicaltrials.gov/show/NCT01043380

Keywords

Versions (1)
  1. 3/2/20 3/2/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 2, 2020

DOI

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License

Creative Commons BY 4.0
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Eligibility Hypercholesterolemia NCT01043380

English

Eligibility Hypercholesterolemia NCT01043380

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed written informed consent,
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
30 to 85 years old,
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
plan to undergo pci and ldl-c >= 100 mg/dl
Description

Percutaneous Coronary Intervention Planned | Serum LDL cholesterol measurement

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C1301732
UMLS CUI [2]
C0428474
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
familial hypercholesterolemia
Description

Hypercholesterolemia, Familial

Data type

boolean

Alias
UMLS CUI [1]
C0020445
being treated with zetia (ezetimibe)
Description

Zetia | ezetimibe

Data type

boolean

Alias
UMLS CUI [1]
C1170736
UMLS CUI [2]
C1142985
being treated with fibrates
Description

Fibrates

Data type

boolean

Alias
UMLS CUI [1]
C1449704
renal insufficiency (serum creatinine >= 2.0 mg/dl)
Description

Renal Insufficiency | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0201976
altered hepatic function (serum aspartate aminotransferase or alanine aminotransferase >= 3-folds of standard value in each institute)
Description

Liver function altered | Aspartate aminotransferase increased | Alanine aminotransferase increased

Data type

boolean

Alias
UMLS CUI [1,1]
C0232741
UMLS CUI [1,2]
C0392747
UMLS CUI [2]
C0151904
UMLS CUI [3]
C0151905
undergoing hemodialysis or peritoneal dialysis
Description

Hemodialysis | Peritoneal Dialysis

Data type

boolean

Alias
UMLS CUI [1]
C0019004
UMLS CUI [2]
C0031139
allergic to lipitor and/or zetia
Description

Hypersensitivity Lipitor | Hypersensitivity Zetia

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0593906
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1170736
severe underlying disease
Description

Primary disorder Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0277554
UMLS CUI [1,2]
C0205082
lack of decision-making capacity
Description

Decision Making Capability Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C0011109
UMLS CUI [1,2]
C2698977
UMLS CUI [1,3]
C0332268
recognized as inadequate by attending doctor
Description

Study Subject Participation Status Inadequate

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0205412
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Similar models

Eligibility Hypercholesterolemia NCT01043380

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
signed written informed consent,
boolean
C0021430 (UMLS CUI [1])
Age
Item
30 to 85 years old,
boolean
C0001779 (UMLS CUI [1])
Percutaneous Coronary Intervention Planned | Serum LDL cholesterol measurement
Item
plan to undergo pci and ldl-c >= 100 mg/dl
boolean
C1532338 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0428474 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Hypercholesterolemia, Familial
Item
familial hypercholesterolemia
boolean
C0020445 (UMLS CUI [1])
Zetia | ezetimibe
Item
being treated with zetia (ezetimibe)
boolean
C1170736 (UMLS CUI [1])
C1142985 (UMLS CUI [2])
Fibrates
Item
being treated with fibrates
boolean
C1449704 (UMLS CUI [1])
Renal Insufficiency | Creatinine measurement, serum
Item
renal insufficiency (serum creatinine >= 2.0 mg/dl)
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver function altered | Aspartate aminotransferase increased | Alanine aminotransferase increased
Item
altered hepatic function (serum aspartate aminotransferase or alanine aminotransferase >= 3-folds of standard value in each institute)
boolean
C0232741 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C0151904 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
Hemodialysis | Peritoneal Dialysis
Item
undergoing hemodialysis or peritoneal dialysis
boolean
C0019004 (UMLS CUI [1])
C0031139 (UMLS CUI [2])
Hypersensitivity Lipitor | Hypersensitivity Zetia
Item
allergic to lipitor and/or zetia
boolean
C0020517 (UMLS CUI [1,1])
C0593906 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1170736 (UMLS CUI [2,2])
Primary disorder Severe
Item
severe underlying disease
boolean
C0277554 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Decision Making Capability Lacking
Item
lack of decision-making capacity
boolean
C0011109 (UMLS CUI [1,1])
C2698977 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Study Subject Participation Status Inadequate
Item
recognized as inadequate by attending doctor
boolean
C2348568 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
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