ID

19902

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

Versies (2)
  1. 30-01-17 30-01-17 -
  2. 14-02-17 14-02-17 -
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30 januari 2017

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Creative Commons BY-NC 3.0
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Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Engels

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

1 Formulieren  
Concomitant Non-Drug Therapy
Beschrijving

Concomitant Non-Drug Therapy

Alias
UMLS CUI-1
C1707479
1. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
1. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
1. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
1. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
2. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
2. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
2. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
2. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
3. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
3. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
3. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
3. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
4. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
4. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
4. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
4. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
5. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
5. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
5. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
5. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
6. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
6. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
6. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
6. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
7. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
7. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
7. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
7. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
8. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
8. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
8. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
8. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
9. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
9. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
9. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
9. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
10. Treatment/ Procedure
Beschrijving

treatment/ procedure

Datatype

text

Alias
UMLS CUI [1]
C0087111
10. Indication
Beschrijving

indication

Datatype

text

Alias
UMLS CUI [1]
C3146298
10. Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
10. Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
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Similar models

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Concomitant Non-Drug Therapy
C1707479 (UMLS CUI-1)
treatment/ procedure
Item
1. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
1. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
1. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
1. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
2. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
2. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
2. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
2. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
3. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
3. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
3. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
3. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
4. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
4. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
4. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
4. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
5. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
5. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
5. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
5. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
6. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
6. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
6. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
6. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
7. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
7. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
7. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
7. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
8. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
8. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
8. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
8. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
9. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
9. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
9. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
9. Stop Date
date
C0806020 (UMLS CUI [1])
treatment/ procedure
Item
10. Treatment/ Procedure
text
C0087111 (UMLS CUI [1])
indication
Item
10. Indication
text
C3146298 (UMLS CUI [1])
start date
Item
10. Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
10. Stop Date
date
C0806020 (UMLS CUI [1])
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