ID

19906

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 -
Geüploaded op

30 januari 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Hospitalization CRFs Multiple Sclerosis Tysabri NCT00027300

Hospitalization CRFs Multiple Sclerosis Tysabri NCT00027300

Hospitalization
Beschrijving

Hospitalization

Alias
UMLS CUI-1
C0019993
Did the subject have any in-patient hospitalizations during the course of the study?
Beschrijving

If Yes, record any inpatient hospitalizations below and complete a Serious Adverse Event form.

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1314939
Line No.
Beschrijving

line number

Datatype

integer

Date of Admission
Beschrijving

date of admission

Datatype

date

Alias
UMLS CUI [1]
C1302393
Date of Discharge
Beschrijving

date of discharge

Datatype

date

Alias
UMLS CUI [1]
C2361123
Primary Reasons for Hospitalization (check one reason for each hospitalization)
Beschrijving

primary reason hospitalization

Datatype

text

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C1549995
If Other, specify:
Beschrijving

other

Datatype

text

Similar models

Hospitalization CRFs Multiple Sclerosis Tysabri NCT00027300

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Hospitalization
C0019993 (UMLS CUI-1)
hospitalization
Item
Did the subject have any in-patient hospitalizations during the course of the study?
boolean
C0019993 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1314939 (UMLS CUI [1,3])
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)
date of admission
Item
Date of Admission
date
C1302393 (UMLS CUI [1])
date of discharge
Item
Date of Discharge
date
C2361123 (UMLS CUI [1])
Item
Primary Reasons for Hospitalization (check one reason for each hospitalization)
text
C0019993 (UMLS CUI [1,1])
C1549995 (UMLS CUI [1,2])
Code List
Primary Reasons for Hospitalization (check one reason for each hospitalization)
CL Item
MS relapse (MS relapse)
CL Item
Other MS related complication (Other MS related complication)
CL Item
Elective surgery (Elective surgery)
CL Item
Other (Other)
other
Item
If Other, specify:
text

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