Informatie:
Fout:
ID
39904
Beschrijving
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
Trefwoorden
Versies (1)
- 02-03-20 02-03-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
2 maart 2020
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypercholesterolemia NCT01043380
Eligibility Hypercholesterolemia NCT01043380
- StudyEvent: Eligibility
Similar models
Eligibility Hypercholesterolemia NCT01043380
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
C1301732 (UMLS CUI [1,2])
C0428474 (UMLS CUI [2])
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])
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])
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])
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])
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])
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])
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])
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])
C0205412 (UMLS CUI [1,2])