ID

15692

Beschrijving

Nerventra Study (Eudra CT 2007-003226-19) Study MS-LAQ-301: A multinational, multicenter, randomized, double-blind, parallel-group, placebo-controlled study, to evaluate the safety, tolerability and efficacy of daily oral administration of laquinimod 0.6 mg in subjects with relapsing remitting multiple sclerosis (RRMS)

Trefwoorden

  1. 08-06-16 08-06-16 -
Geüploaded op

8 juni 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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Nerventra Study Laboratory data

Nerventra Study Laboratory data

Demographic Information
Beschrijving

Demographic Information

Protocol Number
Beschrijving

Protocol Number

Datatype

text

Alias
UMLS CUI [1,1]
C0008971
UMLS CUI [1,2]
C0600091
Visit Type
Beschrijving

i.e "Screening"

Datatype

text

Alias
UMLS CUI [1]
C0545082
Date of visit
Beschrijving

Visit date

Datatype

date

Alias
UMLS CUI [1]
C1320303
Study site number
Beschrijving

Study site

Datatype

integer

Alias
UMLS CUI [1]
C2825164
Subject number:
Beschrijving

Subject number

Datatype

integer

Alias
UMLS CUI [1]
C1709561
No data to report
Beschrijving

Blank

Datatype

boolean

Alias
UMLS CUI [1]
C0750479
Laboratory parameter
Beschrijving

Laboratory parameter

Laboratory parameter
Beschrijving

Laboratory parameter

Datatype

text

Alias
UMLS CUI [1]
C0022885
Date of laboratory test
Beschrijving

Date laboratory

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0022885
Laboratory value
Beschrijving

Value

Datatype

float

Alias
UMLS CUI [1]
C0519835
Unit
Beschrijving

Unit

Datatype

text

Alias
UMLS CUI [1]
C2348328
Normal range upper limit
Beschrijving

Normal range upper limit

Datatype

integer

Alias
UMLS CUI [1,1]
C0086715
UMLS CUI [1,2]
C2827740
Normal range lower limit
Beschrijving

Normal range lower limit

Datatype

integer

Alias
UMLS CUI [1,1]
C0086715
UMLS CUI [1,2]
C2827739

Similar models

Nerventra Study Laboratory data

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Demographic Information
Protocol Number
Item
Protocol Number
text
C0008971 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Visit
Item
Visit Type
text
C0545082 (UMLS CUI [1])
Visit date
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Study site
Item
Study site number
integer
C2825164 (UMLS CUI [1])
Subject number
Item
Subject number:
integer
C1709561 (UMLS CUI [1])
Blank
Item
No data to report
boolean
C0750479 (UMLS CUI [1])
Item Group
Laboratory parameter
Laboratory parameter
Item
Laboratory parameter
text
C0022885 (UMLS CUI [1])
Date laboratory
Item
Date of laboratory test
date
C0011008 (UMLS CUI [1,1])
C0022885 (UMLS CUI [1,2])
Value
Item
Laboratory value
float
C0519835 (UMLS CUI [1])
Unit
Item
Unit
text
C2348328 (UMLS CUI [1])
Normal range upper limit
Item
Normal range upper limit
integer
C0086715 (UMLS CUI [1,1])
C2827740 (UMLS CUI [1,2])
Normal range lower limit
Item
Normal range lower limit
integer
C0086715 (UMLS CUI [1,1])
C2827739 (UMLS CUI [1,2])

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