ID

18286

Description

A Study to Evaluate the Impact on Skin (Injection Site) Reactions of Taking an Antihistamine (Zyrtec®) or Placebo Prior to Daily Injections of Copaxone®.; ODM derived from: https://clinicaltrials.gov/show/NCT00240032

Link

https://clinicaltrials.gov/show/NCT00240032

Keywords

  1. 10/27/16 10/27/16 -
Uploaded on

October 27, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT00240032

Eligibility Multiple Sclerosis NCT00240032

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
18 years of age or older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
diagnosis of rrms
Description

Multiple Sclerosis, Relapsing-Remitting

Data type

boolean

Alias
UMLS CUI [1]
C0751967
beginning or recently (within < 3months) began self-injecting copaxone®
Description

Copaxone Injection Self

Data type

boolean

Alias
UMLS CUI [1,1]
C0528175
UMLS CUI [1,2]
C1828121
UMLS CUI [1,3]
C0036588
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
taking any other immunomodulatory therapy in conjunction with copaxone®
Description

Immunomodulation | Copaxone

Data type

boolean

Alias
UMLS CUI [1]
C1963758
UMLS CUI [2]
C0528175
unable to perform subcutaneous self-injection
Description

Injection Self Subcutaneous Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C1828121
UMLS CUI [1,2]
C0036588
UMLS CUI [1,3]
C1522438
UMLS CUI [1,4]
C1299582
pregnant or trying to become pregnant, or breast feeding during the study
Description

Pregnancy | Pregnancy, Planned | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
UMLS CUI [3]
C0006147
previously participated in this study or in another clinical trial in the past 30 days
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Multiple Sclerosis NCT00240032

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Multiple Sclerosis, Relapsing-Remitting
Item
diagnosis of rrms
boolean
C0751967 (UMLS CUI [1])
Copaxone Injection Self
Item
beginning or recently (within < 3months) began self-injecting copaxone®
boolean
C0528175 (UMLS CUI [1,1])
C1828121 (UMLS CUI [1,2])
C0036588 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Immunomodulation | Copaxone
Item
taking any other immunomodulatory therapy in conjunction with copaxone®
boolean
C1963758 (UMLS CUI [1])
C0528175 (UMLS CUI [2])
Injection Self Subcutaneous Unable
Item
unable to perform subcutaneous self-injection
boolean
C1828121 (UMLS CUI [1,1])
C0036588 (UMLS CUI [1,2])
C1522438 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,4])
Pregnancy | Pregnancy, Planned | Breast Feeding
Item
pregnant or trying to become pregnant, or breast feeding during the study
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Study Subject Participation Status
Item
previously participated in this study or in another clinical trial in the past 30 days
boolean
C2348568 (UMLS CUI [1])

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