Informações:
Falhas:
ID
36575
Descrição
Natural History of Multiple Sclerosis and Its Mimickers; ODM derived from: https://clinicaltrials.gov/show/NCT02504840
Link
https://clinicaltrials.gov/show/NCT02504840
Palavras-chave
Versões (1)
- 22/05/2019 22/05/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
22 de maio de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Neurologic Disorders NCT02504840
Eligibility Neurologic Disorders NCT02504840
- StudyEvent: Eligibility
Similar models
Eligibility Neurologic Disorders NCT02504840
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
ID.1
Item
< tab>
boolean
Inclusion criteria Quantity
Item
one or more of the following:
boolean
C1512693 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
Multiple Sclerosis | Clinically isolated syndrome | Radiologically isolated syndrome
Item
diagnosis of ms, clinically isolated syndrome, or radiologically isolated syndrome.
boolean
C0026769 (UMLS CUI [1])
C2921627 (UMLS CUI [2])
C4324721 (UMLS CUI [3])
C2921627 (UMLS CUI [2])
C4324721 (UMLS CUI [3])
Signs and Symptoms Consistent with Central nervous system demyelination inflammatory | Neuroimaging Consistent with Central nervous system demyelination inflammatory
Item
presentation with clinical or neuroimaging findings that, in the best judgment of the investigators, are possibly consistent with central nervous system inflammatory demyelination.
boolean
C0037088 (UMLS CUI [1,1])
C0332290 (UMLS CUI [1,2])
C0338474 (UMLS CUI [1,3])
C0333348 (UMLS CUI [1,4])
C0679575 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0338474 (UMLS CUI [2,3])
C0333348 (UMLS CUI [2,4])
C0332290 (UMLS CUI [1,2])
C0338474 (UMLS CUI [1,3])
C0333348 (UMLS CUI [1,4])
C0679575 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0338474 (UMLS CUI [2,3])
C0333348 (UMLS CUI [2,4])
Healthy Volunteers
Item
healthy volunteer.
boolean
C1708335 (UMLS CUI [1])
Age
Item
age greater than or equal to18.
boolean
C0001779 (UMLS CUI [1])
Participation Clinical Trial Procedure | Research data with quality Provide
Item
able to participate in study procedures and provide high-quality clinical research data, in the best judgment of the investigators.
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C0681873 (UMLS CUI [2,1])
C0332306 (UMLS CUI [2,2])
C1999230 (UMLS CUI [2,3])
C0008976 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C0681873 (UMLS CUI [2,1])
C0332306 (UMLS CUI [2,2])
C1999230 (UMLS CUI [2,3])
Procedure Quantity Perform
Item
interest of the study investigators in performing one or more procedures under one or more of the substudies.
boolean
C0184661 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,3])
ID.9
Item
< tab>
boolean
Sample Collection Sharing Unwilling | Data Collection Sharing Unwilling
Item
unwilling to allow sharing and/or use in future studies of coded samples and data that are collected for this study.
boolean
C0200345 (UMLS CUI [1,1])
C0237876 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0010995 (UMLS CUI [2,1])
C0237876 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0237876 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0010995 (UMLS CUI [2,1])
C0237876 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
Informed Consent Unable
Item
inability to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])