Eligibility Schizophrenia NCT00169065

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 20-60 years;
Beschreibung

age

Datentyp

boolean

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

schizophrenia or schizoaffective disorder

Datentyp

boolean

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

BPRS

Datentyp

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);
Beschreibung

antipsychotic agents

Datentyp

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;
Beschreibung

informed consent

Datentyp

boolean

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

clozapine or olanzapine

Datentyp

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
current substance abuse;
Beschreibung

substance abuse

Datentyp

boolean

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

suicide or homicide risk

Datentyp

boolean

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

pregnancy, lactation

Datentyp

boolean

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

seizures, blood dyscrasias

Datentyp

boolean

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

Ähnliche Modelle

Eligibility Schizophrenia NCT00169065

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])