ID

21788

Beschrijving

Bifeprunox Extension to Extension Study in Patients With Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00861497

Link

https://clinicaltrials.gov/show/NCT00861497

Trefwoorden

  1. 30-04-17 30-04-17 -
Geüploaded op

30 april 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Schizophrenia NCT00861497

Eligibility Schizophrenia NCT00861497

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients, suffering from schizophrenia, having completed studies 10206 or 10265
Beschrijving

Schizophrenia and Study Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C2348568
otherwise healthy
Beschrijving

Health Status

Datatype

boolean

Alias
UMLS CUI [1]
C0018759
female patients of non-childbearing potential, or non-pregnant, not breast-feeding women using adequate contraception
Beschrijving

Gynaecological Status

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0700589
the patient must be in need of treatment with bifeprunox (that is, the switch to another compound is not feasible)
Beschrijving

Bifeprunox

Datatype

boolean

Alias
UMLS CUI [1]
C1721449
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
current axis i primary psychiatric diagnosis other than schizophrenia
Beschrijving

Axis I Diagnosis

Datatype

boolean

Alias
UMLS CUI [1]
C0270287
significant risk of suicide and/or violent behaviour
Beschrijving

Suicidal ideation or violent behaviour

Datatype

boolean

Alias
UMLS CUI [1]
C0424000
UMLS CUI [2]
C0424323
other psychiatric, neurological or behavioural disorders that may interfere with study conduct
Beschrijving

Psychiatric, neurological or behavioural disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0004936
UMLS CUI [2]
C0027765
UMLS CUI [3]
C0004930
substance or alcohol abuse, current cannabis dependence
Beschrijving

Substance Use Disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0038586
clinically significant physical illness
Beschrijving

Comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488

Similar models

Eligibility Schizophrenia NCT00861497

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Schizophrenia and Study Participation Status
Item
patients, suffering from schizophrenia, having completed studies 10206 or 10265
boolean
C0036341 (UMLS CUI [1])
C2348568 (UMLS CUI [2])
Health Status
Item
otherwise healthy
boolean
C0018759 (UMLS CUI [1])
Gynaecological Status
Item
female patients of non-childbearing potential, or non-pregnant, not breast-feeding women using adequate contraception
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])
Bifeprunox
Item
the patient must be in need of treatment with bifeprunox (that is, the switch to another compound is not feasible)
boolean
C1721449 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Axis I Diagnosis
Item
current axis i primary psychiatric diagnosis other than schizophrenia
boolean
C0270287 (UMLS CUI [1])
Suicidal ideation or violent behaviour
Item
significant risk of suicide and/or violent behaviour
boolean
C0424000 (UMLS CUI [1])
C0424323 (UMLS CUI [2])
Psychiatric, neurological or behavioural disorders
Item
other psychiatric, neurological or behavioural disorders that may interfere with study conduct
boolean
C0004936 (UMLS CUI [1])
C0027765 (UMLS CUI [2])
C0004930 (UMLS CUI [3])
Substance Use Disorders
Item
substance or alcohol abuse, current cannabis dependence
boolean
C0038586 (UMLS CUI [1])
Comorbidity
Item
clinically significant physical illness
boolean
C0009488 (UMLS CUI [1])

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