18 years old or older
Item
must be 18 years old or above.
boolean
C0001779 (UMLS CUI [1])
schizophrenia or schizoaffective disorder
Item
clinical diagnosis of schizophrenia or schizoaffective disorder
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
positive and-negative syndrome score (panss)
Item
must be with a stable mental status as demonstrated by a stable positive and-negative symptom score (panss) score over a period of 2 weeks.
boolean
C0451383 (UMLS CUI [1])
medication changes
Item
must have no medication changes in the 2 weeks prior to obtaining informed consent.
boolean
C0013227 (UMLS CUI [1,1])
C0580105 (UMLS CUI [1,2])
inability to give informed consent; unable to give informed consent
Item
must be able to give informed consent for the trial.
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
unwilling or unable, in the opinion of the investigator, to comply with study instructions
boolean
C0525058 (UMLS CUI [1])
breast-feeding; pregnant
Item
pregnant or breast-feeding.
boolean
C0006147 (UMLS CUI [1])
C0549206 (UMLS CUI [2])
dsm-v substance ; alcohol abuse.
Item
current dsm-v substance or alcohol abuse.
boolean
C0038586 (UMLS CUI [1])
C1137105 (UMLS CUI [2,1])
C0439861 (UMLS CUI [2,2])
delirium
Item
concurrent delirium
boolean
C0011206 (UMLS CUI [1])
mental retardation
Item
mental retardation
boolean
C0004936 (UMLS CUI [1])
drug-induced psychosis
Item
drug-induced psychosis
boolean
C0033937 (UMLS CUI [1])
significant brain trauma
Item
history of clinically significant brain trauma documented by ct or mri.
boolean
C0876926 (UMLS CUI [1])
epilepsy or had seizures
Item
epilepsy or had seizures 6 months prior the beginning of the study
boolean
C0014544 (UMLS CUI [1])
C0036572 (UMLS CUI [2])