ID

20217

Beschrijving

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.

Trefwoorden

  1. 30-01-17 30-01-17 -
  2. 14-02-17 14-02-17 -
Geüploaded op

14 februari 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Concomitant Non-Drug Therapy
Beschrijving

Concomitant Non-Drug Therapy

Alias
UMLS CUI-1
C1707479
Treatment/ Procedure
Beschrijving

Treatment/ Procedure

Datatype

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1707479
Indication
Beschrijving

Indication

Datatype

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0087111
Start Date
Beschrijving

Start Date

Datatype

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0087111
Continuing
Beschrijving

Continuing

Datatype

boolean

Alias
UMLS CUI [1,1]
C1553904
UMLS CUI [1,2]
C0087111

Similar models

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Concomitant Non-Drug Therapy
C1707479 (UMLS CUI-1)
Item
Treatment/ Procedure
text
C0087111 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Code List
Treatment/ Procedure
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)
Item
Indication
text
C3146298 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Code List
Indication
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)
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Continuing
Item
Continuing
boolean
C1553904 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial