Base Clinical Trial
Item
base study:
boolean
C1705938 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
Coronary heart disease | Disease Risk Equivalent | Statin | LDL Cholesterol Well controlled
Item
patient has coronary heart disease (chd) or chd risk-equivalent disease and is treated with a statin, with well controlled ldl-c
boolean
C0010068 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0035647 (UMLS CUI [2,2])
C0205163 (UMLS CUI [2,3])
C0360714 (UMLS CUI [3])
C0023824 (UMLS CUI [4,1])
C3853142 (UMLS CUI [4,2])
Extension Clinical Trial
Item
extension study:
boolean
C0231448 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
Base Clinical Trial Completed | Reversibility Time period Including
Item
patient has completed the base study including the reversibility period (i.e. 12 or to up to 24 weeks).
boolean
C1705938 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C0449261 (UMLS CUI [2,1])
C1948053 (UMLS CUI [2,2])
C0332257 (UMLS CUI [2,3])
Statins | LIPID MODIFYING AGENTS
Item
patient is on statin therapy ± lipid-modifying therapy since the end of the base study and planning to continue taking a statin throughout the study
boolean
C0360714 (UMLS CUI [1])
C3653535 (UMLS CUI [2])
Heart failure | Cardiac Arrhythmia | Myocardial Infarction | Angina, Unstable | Cerebrovascular accident | Blood Pressure Uncontrolled | Hypercholesterolemia Uncontrolled | Liver diseases
Item
history of heart failure, arrhythmias, heart attack, unstable angina, or stroke within 3 months prior to screening, uncontrolled blood pressure, uncontrolled high cholesterol or liver disease.
boolean
C0018801 (UMLS CUI [1])
C0003811 (UMLS CUI [2])
C0027051 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0038454 (UMLS CUI [5])
C0005823 (UMLS CUI [6,1])
C0205318 (UMLS CUI [6,2])
C0020443 (UMLS CUI [7,1])
C0205318 (UMLS CUI [7,2])
C0023895 (UMLS CUI [8])
Instability mental | Substance Use Disorders
Item
history of mental instability, drug/alcohol abuse within the past 5 years
boolean
C1444783 (UMLS CUI [1,1])
C0229992 (UMLS CUI [1,2])
C0038586 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Malignant Neoplasms
Item
history of cancer within the last 5 years
boolean
C0006826 (UMLS CUI [1])
HIV Seropositivity
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])
Blood Donation
Item
donated blood products within 8 weeks
boolean
C0005794 (UMLS CUI [1])
Study Subject Participation Status | Compound Investigational
Item
currently participating or have participated in a study with an investigational compound within the last 30 days
boolean
C2348568 (UMLS CUI [1])
C1706082 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])