Information:
Fel:
ID
19942
Beskrivning
Vytorin Treating Uncontrolled Lipids (VyTUL) Study (TERMINATED); ODM derived from: https://clinicaltrials.gov/show/NCT00395603
Länk
https://clinicaltrials.gov/show/NCT00395603
Nyckelord
Versioner (1)
- 2017-01-31 2017-01-31 -
Uppladdad den
31 januari 2017
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Cardiovascular Diseases NCT00395603
Eligibility Cardiovascular Diseases NCT00395603
- StudyEvent: Eligibility
Similar models
Eligibility Cardiovascular Diseases NCT00395603
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age
Item
greater than 18 years of age
boolean
C0001779 (UMLS CUI [1])
atorvastatin Dose U/day
Item
treated for at least the last 3 months with a daily dose of atorvastatin 40 mg
boolean
C0286651 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456683 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C0456683 (UMLS CUI [1,3])
Coronary heart disease | Cholesterol measurement
Item
existing coronary heart disease and cholesterol > 4.0 mmol/l
boolean
C0010068 (UMLS CUI [1])
C0201950 (UMLS CUI [2])
C0201950 (UMLS CUI [2])
Diabetic - poor control
Item
uncontrolled diabetes
boolean
C0421258 (UMLS CUI [1])
Increased liver function tests
Item
elevated liver function tests
boolean
C0877359 (UMLS CUI [1])
Elevated creatine kinase
Item
elevated creatine kinase (ck)
boolean
C0151576 (UMLS CUI [1])
Triglycerides measurement
Item
triglycerides (tg) > 4.5 mmol/l
boolean
C0202236 (UMLS CUI [1])
Substance Dependence
Item
drug or alcohol dependency within 6 months prior to visit 1
boolean
C0038580 (UMLS CUI [1])
Gender Hormone Therapy Unstable | Continuing therapy Willing
Item
woman receiving hormonal therapy who have not been maintained on a stable dose and regimen for at least 8 weeks and are willing to continue the same regimen for the duration of the study
boolean
C0079399 (UMLS CUI [1,1])
C0279025 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,3])
C1553904 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
C0279025 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,3])
C1553904 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
Childbearing Potential Contraceptive methods Lacking
Item
woman of childbearing potential not using an acceptable method of birth control
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C0700589 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
women who are pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])