ID

36575

Description

Natural History of Multiple Sclerosis and Its Mimickers; ODM derived from: https://clinicaltrials.gov/show/NCT02504840

Link

https://clinicaltrials.gov/show/NCT02504840

Keywords

  1. 5/22/19 5/22/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 22, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Neurologic Disorders NCT02504840

Eligibility Neurologic Disorders NCT02504840

Criteria
Description

Criteria

< tab>
Description

ID.1

Data type

boolean

one or more of the following:
Description

Inclusion criteria Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1265611
diagnosis of ms, clinically isolated syndrome, or radiologically isolated syndrome.
Description

Multiple Sclerosis | Clinically isolated syndrome | Radiologically isolated syndrome

Data type

boolean

Alias
UMLS CUI [1]
C0026769
UMLS CUI [2]
C2921627
UMLS CUI [3]
C4324721
presentation with clinical or neuroimaging findings that, in the best judgment of the investigators, are possibly consistent with central nervous system inflammatory demyelination.
Description

Signs and Symptoms Consistent with Central nervous system demyelination inflammatory | Neuroimaging Consistent with Central nervous system demyelination inflammatory

Data type

boolean

Alias
UMLS CUI [1,1]
C0037088
UMLS CUI [1,2]
C0332290
UMLS CUI [1,3]
C0338474
UMLS CUI [1,4]
C0333348
UMLS CUI [2,1]
C0679575
UMLS CUI [2,2]
C0332290
UMLS CUI [2,3]
C0338474
UMLS CUI [2,4]
C0333348
healthy volunteer.
Description

Healthy Volunteers

Data type

boolean

Alias
UMLS CUI [1]
C1708335
age greater than or equal to18.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
able to participate in study procedures and provide high-quality clinical research data, in the best judgment of the investigators.
Description

Participation Clinical Trial Procedure | Research data with quality Provide

Data type

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0184661
UMLS CUI [2,1]
C0681873
UMLS CUI [2,2]
C0332306
UMLS CUI [2,3]
C1999230
interest of the study investigators in performing one or more procedures under one or more of the substudies.
Description

Procedure Quantity Perform

Data type

boolean

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0884358
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
< tab>
Description

ID.9

Data type

boolean

unwilling to allow sharing and/or use in future studies of coded samples and data that are collected for this study.
Description

Sample Collection Sharing Unwilling | Data Collection Sharing Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0237876
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C0010995
UMLS CUI [2,2]
C0237876
UMLS CUI [2,3]
C0558080
inability to provide informed consent.
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582

Similar models

Eligibility Neurologic Disorders NCT02504840

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
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])
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])
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])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
Informed Consent Unable
Item
inability to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])

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