ID

19903

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 -
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30 januari 2017

DOI

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Creative Commons BY-NC 3.0

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Alternate MS Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Alternate MS Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Alternate MS Therapy
Beschrijving

Alternate MS Therapy

Alias
UMLS CUI-1
C0949216
1. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
1. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
1. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
1. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
2. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
2. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
2. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
3. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
3. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
3. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
4. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
4. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
4. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
5. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
5. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
5. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
6. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
6. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
6. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
7. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
7. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
7. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
8. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
8. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
9. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
9. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
9. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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. Medication Name
Beschrijving

medication name

Datatype

text

Alias
UMLS CUI [1]
C2360065
10. Dose/ Units
Beschrijving

dose

Datatype

text

Alias
UMLS CUI [1]
C3174092
10. Route
Beschrijving

route

Datatype

text

Alias
UMLS CUI [1]
C0013153
10. Frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
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

Similar models

Alternate MS Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Alternate MS Therapy
C0949216 (UMLS CUI-1)
medication name
Item
1. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
1. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
1. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
1. Frequency
text
C3476109 (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])
medication name
Item
2. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
2. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
2. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
2. Frequency
text
C3476109 (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])
medication name
Item
3. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
3. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
3. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
3. Frequency
text
C3476109 (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])
medication name
Item
4. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
4. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
4. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
4. Frequency
text
C3476109 (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])
medication name
Item
5. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
5. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
5. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
5. Frequency
text
C3476109 (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])
medication name
Item
6. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
6. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
6. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
6. Frequency
text
C3476109 (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])
medication name
Item
7. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
7. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
7. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
7. Frequency
text
C3476109 (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])
medication name
Item
8. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
8. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
8. Route
text
C0013153 (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])
medication name
Item
9. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
9. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
9. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
9. Frequency
text
C3476109 (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])
medication name
Item
10. Medication Name
text
C2360065 (UMLS CUI [1])
dose
Item
10. Dose/ Units
text
C3174092 (UMLS CUI [1])
route
Item
10. Route
text
C0013153 (UMLS CUI [1])
frequency
Item
10. Frequency
text
C3476109 (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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