ID

19909

Description

The purpose of this study is to determine the safety and efficacy of natalizumab in the treatment of individuals who have been diagnosed with relapsing remitting multiple sclerosis (MS). It is hoped that natalizumab will prevent certain types of white blood cells from moving out of the bloodstream into organs, including the brain, that are being damaged by autoimmune disease (a disease in which the body's own immune system attacks certain organs). These white blood cells are thought to cause inflammation that can result in lesions (small areas of damage) in the brain. These lesions are thought to be the cause of relapses and disability in MS. Documentation process: This form is to be obtained in week 0.

Mots-clés

  1. 30/01/2017 30/01/2017 -
Téléchargé le

30 janvier 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Baseline Signs and Symptoms CRFs Multiple Sclerosis Tysabri NCT00027300

Baseline Signs and Symptoms CRFs Multiple Sclerosis Tysabri NCT00027300

Baseline Signs and Symptoms
Description

Baseline Signs and Symptoms

Alias
UMLS CUI-1
C0037088
Line No.
Description

Line Number

Type de données

integer

Sign or Symptom
Description

Sign or Symptom

Type de données

text

Alias
UMLS CUI [1]
C3540840
Start Date
Description

Start Date

Type de données

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Stop Date

Type de données

date

Alias
UMLS CUI [1]
C0806020
Not Resolved
Description

Not Resolved

Type de données

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1709863
Severity
Description

Severity

Type de données

integer

Alias
UMLS CUI [1]
C0439793

Similar models

Baseline Signs and Symptoms CRFs Multiple Sclerosis Tysabri NCT00027300

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Baseline Signs and Symptoms
C0037088 (UMLS CUI-1)
Item
Line No.
integer
Code List
Line No.
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
CL Item
8 (8)
CL Item
9 (9)
CL Item
10 (10)
Sign or Symptom
Item
Sign or Symptom
text
C3540840 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Item
Not Resolved
integer
C0877248 (UMLS CUI [1,1])
C1709863 (UMLS CUI [1,2])
Code List
Not Resolved
CL Item
Not Resolved (1)
Item
Severity
integer
C0439793 (UMLS CUI [1])
Code List
Severity
CL Item
Mild (1)
CL Item
Moderate (2)
CL Item
Severe (3)

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