ID

34565

Descrição

Efficiency Study to Investigate Blonanserin in Treatment of Schizophrenia When Compared With Risperidone; ODM derived from: https://clinicaltrials.gov/show/NCT01516424

Link

https://clinicaltrials.gov/show/NCT01516424

Palavras-chave

  1. 19/01/2019 19/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

19 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Schizophrenia NCT01516424

Eligibility Schizophrenia NCT01516424

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject met dsm-iv-tr criteria for a primary diagnosis of schizophrenia
Descrição

ID.1

Tipo de dados

boolean

patients are 18≤age≤65 years of age on the day when informed consent is obtained.
Descrição

ID.2

Tipo de dados

boolean

subject had a panss total score ≥70 and 120≥ at screening
Descrição

ID.3

Tipo de dados

boolean

subject had a score ≥4 on the panss at screening and baseline.
Descrição

ID.4

Tipo de dados

boolean

subjects are willing and able to comply with study protocol including treatment in hospital.
Descrição

ID.5

Tipo de dados

boolean

subjects or their legal guardians have signed the written informed consent form.
Descrição

ID.6

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
the subject was treatment with other investigate product within 30 days.
Descrição

ID.7

Tipo de dados

boolean

subject had a history of treatment with long-acting drug for anti schizophrenia within 56 days.
Descrição

ID.8

Tipo de dados

boolean

subject had a history of treatment with clozapine within 28 days.
Descrição

ID.9

Tipo de dados

boolean

subject with parkinson disease,etc
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Schizophrenia NCT01516424

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subject met dsm-iv-tr criteria for a primary diagnosis of schizophrenia
boolean
ID.2
Item
patients are 18≤age≤65 years of age on the day when informed consent is obtained.
boolean
ID.3
Item
subject had a panss total score ≥70 and 120≥ at screening
boolean
ID.4
Item
subject had a score ≥4 on the panss at screening and baseline.
boolean
ID.5
Item
subjects are willing and able to comply with study protocol including treatment in hospital.
boolean
ID.6
Item
subjects or their legal guardians have signed the written informed consent form.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
the subject was treatment with other investigate product within 30 days.
boolean
ID.8
Item
subject had a history of treatment with long-acting drug for anti schizophrenia within 56 days.
boolean
ID.9
Item
subject had a history of treatment with clozapine within 28 days.
boolean
ID.10
Item
subject with parkinson disease,etc
boolean

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