Age
Item
male and female subjects ages 18-65 years
boolean
C0001779 (UMLS CUI [1])
Outpatients | Hospital patients Partial Stable
Item
outpatients and stable partial hospital patients
boolean
C0029921 (UMLS CUI [1])
C0021562 (UMLS CUI [2,1])
C0728938 (UMLS CUI [2,2])
C0205360 (UMLS CUI [2,3])
Schizophrenia | Schizoaffective Disorder
Item
diagnostic and statistical manual of mental disorders, fourth edition, text revision (dsm-iv-tr) diagnosis of schizophrenia or schizoaffective disorder
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
psychiatric hospitalization
Item
no psychiatric hospitalization in 30 days prior to study start
boolean
C0748061 (UMLS CUI [1])
Patient in partial remission | Positive and negative syndrome scale
Item
partially remitted patients with a panss score below 100 at screening
boolean
C1562651 (UMLS CUI [1])
C0451383 (UMLS CUI [2])
Antipsychotic Agent Singular Dose Stable
Item
currently on a stable dose of only one antipsychotic for at least 30 days prior to study start
boolean
C0040615 (UMLS CUI [1,1])
C0205171 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0205360 (UMLS CUI [1,4])
Psychotropic Drugs Dose Stable
Item
currently receiving a stable dose of all other psychotropic medications for at least 30 days prior to study start
boolean
C0033978 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Body mass index
Item
bmi greater than 26
boolean
C1305855 (UMLS CUI [1])
Childbearing Potential Contraceptive methods
Item
female patients of childbearing age must be using an acceptable method of birth control for at least 1 month prior to participation in the research study and continue for at least 4 weeks after the final study visit.
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
ability to provide informed consent.
boolean
C0021430 (UMLS CUI [1])
Mental Retardation
Item
mental retardation
boolean
C0025362 (UMLS CUI [1])
Clozapine
Item
current treatment with clozapine
boolean
C0009079 (UMLS CUI [1])
Weight Reduction Program | Weight reduction regimen pharmacological
Item
currently enrolled in a weight management program or receiving pharmacological treatment for weight reduction
boolean
C3179079 (UMLS CUI [1])
C0311130 (UMLS CUI [2,1])
C0205464 (UMLS CUI [2,2])
Illness Serious | Illness Unstable
Item
serious or unstable medical illness
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0221423 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female patients who are pregnant, lactating, or plan to become pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Ketoconazole | Quinidine | Carbamazepine
Item
concurrently receiving treatment with ketoconazole, quinidine, carbamazepine.
boolean
C0022625 (UMLS CUI [1])
C0034414 (UMLS CUI [2])
C0006949 (UMLS CUI [3])