ID

19902

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.

Keywords

Versions (2)
  1. 1/30/17 1/30/17 -
  2. 2/14/17 2/14/17 -
Uploaded on

January 30, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

English

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

1 forms  
Concomitant Non-Drug Therapy
Description

Concomitant Non-Drug Therapy

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
1. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
2. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
3. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
4. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
5. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
6. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
7. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
8. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
9. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

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

treatment/ procedure

Data type

text

Alias
UMLS CUI [1]
C0087111
10. Indication
Description

indication

Data type

text

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

start date

Data type

date

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

stop date

Data type

date

Alias
UMLS CUI [1]
C0806020
Back to the top of the page

Similar models

Concomitant Non-Drug Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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