Stable status Clinical | Antipsychotic Agents Dose
Item
patient is clinically stable, on current antipsychotic medication for at least 3 months and current dose for 2 months
boolean
C0205360 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0040615 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
Reading Grade Level
Item
patient has a 6th grade reading level or better
boolean
C0034754 (UMLS CUI [1,1])
C0870612 (UMLS CUI [1,2])
Pregnancy Absent | Childbearing Potential Sexual Abstinence | Childbearing Potential Contraceptive methods
Item
females are not pregnant, and those who can have children agree to remain abstinent or use acceptable birth control throughout the study
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C3831118 (UMLS CUI [2,1])
C0036899 (UMLS CUI [2,2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
Living Arrangement Stable
Item
patient has had a stable living arrangement for at least 3 months prior to study start
boolean
C0242487 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
General health good
Item
patient is in general good health based on screening assessments
boolean
C1277245 (UMLS CUI [1])
Positive and negative syndrome scale
Item
patient has total positive and negative syndrome scale (panss) score between 36 and 75 at screening and at the first baseline visit
boolean
C0451383 (UMLS CUI [1])
Clinical Global Impression Questionnaire
Item
patient has a clinical global impressions - severity (cgi-s) score less than or equal to 4 at screening and at the first baseline visit
boolean
C3639708 (UMLS CUI [1])
Disease Major | Interference Testing Cognitive | Mental Retardation | Disease Major At risk Study Subject Participation Status
Item
patient has a major disease/disorder that may interfere with cognitive testing (such as mental retardation) and/or pose a risk upon study participation
boolean
C0012634 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0521102 (UMLS CUI [2,1])
C0039593 (UMLS CUI [2,2])
C1516691 (UMLS CUI [2,3])
C0025362 (UMLS CUI [3])
C0012634 (UMLS CUI [4,1])
C0205164 (UMLS CUI [4,2])
C1444641 (UMLS CUI [4,3])
C2348568 (UMLS CUI [4,4])
Craniocerebral Trauma | Unconscious State Duration
Item
patient has a history of head trauma with loss of consciousness greater than 15 minutes
boolean
C0018674 (UMLS CUI [1])
C0041657 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Warfarin | Monoamine Oxidase Inhibitors | Clonazepam | Clozapine
Item
patient has had warfarin treatment, mao inhibitors, clonazepam or clozapine within 1 month of screening
boolean
C0043031 (UMLS CUI [1])
C0026457 (UMLS CUI [2])
C0009011 (UMLS CUI [3])
C0009079 (UMLS CUI [4])
Electroconvulsive Therapy
Item
patient has had ect treatment within 6 months of screening
boolean
C0013806 (UMLS CUI [1])
Antihistamines Patient need for | Pharmaceutical Preparations Study Protocol Patient need for
Item
patient requires treatment with antihistamines or certain other medications listed in the protocol
boolean
C0019590 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C0686904 (UMLS CUI [2,3])
Liver disease | Malignant Neoplasm
Item
patient has a history of liver disease that has been active within the last 2 years, or a history of cancer within the past 5 years
boolean
C0023895 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
Substance Dependence | Substance Use Disorders
Item
patient has a history of alcohol or drug dependence within the past year or alcohol or drug abuse within 3 months of screening
boolean
C0038580 (UMLS CUI [1])
C0038586 (UMLS CUI [2])