Eligibility Schizophrenia NCT00169065

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 20-60 years;
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
diagnosis of treatment refractory schizophrenia or schizoaffective disorder;
Descrizione

schizophrenia or schizoaffective disorder

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0036337
bprs score > 21 (0-6) scale;
Descrizione

BPRS

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0029941
either two 6-8 week trials of typical neuroleptics given at a dosage of 600 mg/day of cpz or its equivalent or one 6-8 week trial of an atypical antipsychotic at a reasonable dose (i.e. risperidone 4-6 mg/day);
Descrizione

antipsychotic agents

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0040615
the patient (or the patient's authorized legal representative) must understand the nature of the study and sign the informed consent;
Descrizione

informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
clinically appropriate for clozapine or olanzapine
Descrizione

clozapine or olanzapine

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009079
UMLS CUI [2]
C0171023
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
current substance abuse;
Descrizione

substance abuse

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038586
suicide or homicide risk;
Descrizione

suicide or homicide risk

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0038661
UMLS CUI [2]
C0019872
pregnancy or lactation;
Descrizione

pregnancy, lactation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
history of seizures or blood dyscrasias
Descrizione

seizures, blood dyscrasias

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0036572
UMLS CUI [2]
C0018939

Similar models

Eligibility Schizophrenia NCT00169065

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age 20-60 years;
boolean
C0001779 (UMLS CUI [1])
schizophrenia or schizoaffective disorder
Item
diagnosis of treatment refractory schizophrenia or schizoaffective disorder;
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
BPRS
Item
bprs score > 21 (0-6) scale;
boolean
C0029941 (UMLS CUI [1])
antipsychotic agents
Item
either two 6-8 week trials of typical neuroleptics given at a dosage of 600 mg/day of cpz or its equivalent or one 6-8 week trial of an atypical antipsychotic at a reasonable dose (i.e. risperidone 4-6 mg/day);
boolean
C0040615 (UMLS CUI [1])
informed consent
Item
the patient (or the patient's authorized legal representative) must understand the nature of the study and sign the informed consent;
boolean
C0021430 (UMLS CUI [1])
clozapine or olanzapine
Item
clinically appropriate for clozapine or olanzapine
boolean
C0009079 (UMLS CUI [1])
C0171023 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
substance abuse
Item
current substance abuse;
boolean
C0038586 (UMLS CUI [1])
suicide or homicide risk
Item
suicide or homicide risk;
boolean
C0038661 (UMLS CUI [1])
C0019872 (UMLS CUI [2])
pregnancy, lactation
Item
pregnancy or lactation;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
seizures, blood dyscrasias
Item
history of seizures or blood dyscrasias
boolean
C0036572 (UMLS CUI [1])
C0018939 (UMLS CUI [2])