ID

14625

Descrição

CARE Study: Improving Treatment for the Most Severely Ill With Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00272584

Link

https://clinicaltrials.gov/show/NCT00272584

Palavras-chave

  1. 24/04/2016 24/04/2016 -
Transferido a

24 de abril de 2016

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Psychosis, Schizophrenia NCT00272584

Eligibility Psychosis, Schizophrenia NCT00272584

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects treated with clozapine for the indication of poor response to other antipsychotic medications.
Descrição

clozapine

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0009079
treatment with clozapine is at a stable dose for at least 12 weeks. dose must be 400 mg/day or more, unless side effects limited increase of dose.
Descrição

treatment with clozapine stable dose

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0009079
UMLS CUI [1,2]
C0205360
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with significant alcohol or substance abuse in the past 3 months.
Descrição

alcohol or substance abuse

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0038586
subjects with a previous trial of risperidone augmentation of clozapine
Descrição

risperidone augmentation

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0073393
UMLS CUI [1,2]
C0442805
UMLS CUI [1,3]
C0205156
subjects who are pregnant, breast-feeding, or women of child-bearing potential not using adequate contraception
Descrição

pregnancy and contraceptive methods

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0700589
UMLS CUI [3]
C0006147
subjects requiring treatment with anticonvulsants.
Descrição

anticonvulsants

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0003286
subjects with known hypersensitivity or allergy to risperidone.
Descrição

allergy to risperidone

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0073393
subjects with hematological or other contraindications to continued clozapine treatment.
Descrição

contraindications to continued clozapine treatment

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0009079

Similar models

Eligibility Psychosis, Schizophrenia NCT00272584

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
clozapine
Item
subjects treated with clozapine for the indication of poor response to other antipsychotic medications.
boolean
C0009079 (UMLS CUI [1])
treatment with clozapine stable dose
Item
treatment with clozapine is at a stable dose for at least 12 weeks. dose must be 400 mg/day or more, unless side effects limited increase of dose.
boolean
C0009079 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
alcohol or substance abuse
Item
subjects with significant alcohol or substance abuse in the past 3 months.
boolean
C0038586 (UMLS CUI [1])
risperidone augmentation
Item
subjects with a previous trial of risperidone augmentation of clozapine
boolean
C0073393 (UMLS CUI [1,1])
C0442805 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
pregnancy and contraceptive methods
Item
subjects who are pregnant, breast-feeding, or women of child-bearing potential not using adequate contraception
boolean
C0032961 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
anticonvulsants
Item
subjects requiring treatment with anticonvulsants.
boolean
C0003286 (UMLS CUI [1])
allergy to risperidone
Item
subjects with known hypersensitivity or allergy to risperidone.
boolean
C0020517 (UMLS CUI [1,1])
C0073393 (UMLS CUI [1,2])
contraindications to continued clozapine treatment
Item
subjects with hematological or other contraindications to continued clozapine treatment.
boolean
C1301624 (UMLS CUI [1,1])
C0009079 (UMLS CUI [1,2])

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