Informações:
Falhas:
ID
39329
Descrição
Stem Cell Research on Subjects at Genetic High Risk for Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT01943175
Link
https://clinicaltrials.gov/show/NCT01943175
Palavras-chave
Versões (1)
- 20/12/2019 20/12/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
20 de dezembro de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Genetic High Risk for Schizophrenia NCT01943175
Eligibility Genetic High Risk for Schizophrenia NCT01943175
- StudyEvent: Eligibility
Similar models
Eligibility Genetic High Risk for Schizophrenia NCT01943175
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Genetic Risk High Schizophrenia
Item
[subjects at genetic high risk for schizophrenia]
boolean
C1517512 (UMLS CUI [1,1])
C0205250 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
C0205250 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
Healthy | Axis I diagnosis Absent
Item
healthy without any axis i mental disorder
boolean
C3898900 (UMLS CUI [1])
C0270287 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0270287 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Monozygotic twin Patient Schizophrenia | Family member Quantity Schizophrenia | First Degree Relative Quantity Schizophrenia
Item
is a monozygotic twin of a patient with schizophrenia or has at least two family members of schizophrenia in the pedigree, including at least one 1st-degree family member
boolean
C0041432 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
C0086282 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0036341 (UMLS CUI [2,3])
C1517194 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0036341 (UMLS CUI [3,3])
C0030705 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
C0086282 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0036341 (UMLS CUI [2,3])
C1517194 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0036341 (UMLS CUI [3,3])
Healthy Control
Item
[healthy control]
boolean
C2986479 (UMLS CUI [1])
Healthy | Axis I diagnosis Absent
Item
healthy without any axis i mental disorder
boolean
C3898900 (UMLS CUI [1])
C0270287 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0270287 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Absence Family member Schizophrenia
Item
no family members of schizophrenia in the pedigree to the 3rd degree
boolean
C0332197 (UMLS CUI [1,1])
C0086282 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
C0086282 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
Nervous system disorder | Illness Clinical Significance
Item
significant neurological or medical illness
boolean
C0027765 (UMLS CUI [1])
C0221423 (UMLS CUI [2,1])
C2826293 (UMLS CUI [2,2])
C0221423 (UMLS CUI [2,1])
C2826293 (UMLS CUI [2,2])
Psychotic symptom
Item
psychotic symptoms
boolean
C0871189 (UMLS CUI [1])
Substance Use Disorders
Item
substance abuse
boolean
C0038586 (UMLS CUI [1])
At risk for suicide
Item
suicidal risk
boolean
C0563664 (UMLS CUI [1])
Blindness | Deafness
Item
blindness or hearing loss
boolean
C0456909 (UMLS CUI [1])
C0011053 (UMLS CUI [2])
C0011053 (UMLS CUI [2])
Aspirin | Warfarin | Hormone Therapy Agent
Item
taking aspirin, warfarin or hormonal agents
boolean
C0004057 (UMLS CUI [1])
C0043031 (UMLS CUI [2])
C0279025 (UMLS CUI [3,1])
C0450442 (UMLS CUI [3,2])
C0043031 (UMLS CUI [2])
C0279025 (UMLS CUI [3,1])
C0450442 (UMLS CUI [3,2])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Susceptibility KELOID FORMATION
Item
susceptibility for keloid formation
boolean
C1264642 (UMLS CUI [1,1])
C3149494 (UMLS CUI [1,2])
C3149494 (UMLS CUI [1,2])
Lidocaine allergy
Item
allergy to lidocaine
boolean
C0570646 (UMLS CUI [1])
Craniocerebral Trauma | History of loss of consciousness
Item
history of significant head trauma or loss of consciousness
boolean
C0018674 (UMLS CUI [1])
C0848041 (UMLS CUI [2])
C0848041 (UMLS CUI [2])
Mental Retardation
Item
mental retardation
boolean
C0025362 (UMLS CUI [1])