Informatie:
Fout:
ID
18286
Beschrijving
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
Trefwoorden
Versies (1)
- 27-10-16 27-10-16 -
Geüploaded op
27 oktober 2016
DOI
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Licentie
Creative Commons BY 4.0
Model Commentaren :
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Eligibility Multiple Sclerosis NCT00240032
Eligibility Multiple Sclerosis NCT00240032
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Sclerosis NCT00240032
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
C1828121 (UMLS CUI [1,2])
C0036588 (UMLS CUI [1,3])
Immunomodulation | Copaxone
Item
taking any other immunomodulatory therapy in conjunction with copaxone®
boolean
C1963758 (UMLS CUI [1])
C0528175 (UMLS CUI [2])
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])
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])
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])