ID

19903

Beschreibung

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.

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  1. 30.01.17 30.01.17 -
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30. Januar 2017

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Alternate MS Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

Englisch

Alternate MS Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

1 Formulare  
Alternate MS Therapy
Beschreibung

Alternate MS Therapy

Alias
UMLS CUI-1
C0949216
1. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
1. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
1. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
1. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
2. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
2. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
2. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
2. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
3. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
3. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
3. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
3. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
4. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
4. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
4. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
4. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
5. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
5. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
5. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
5. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
6. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
6. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
6. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
6. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
7. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
7. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
7. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
7. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
8. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
8. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
8. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
9. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
9. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
9. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
9. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
10. Medication Name
Beschreibung

medication name

Datentyp

text

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

dose

Datentyp

text

Alias
UMLS CUI [1]
C3174092
10. Route
Beschreibung

route

Datentyp

text

Alias
UMLS CUI [1]
C0013153
10. Frequency
Beschreibung

frequency

Datentyp

text

Alias
UMLS CUI [1]
C3476109
10. Start Date
Beschreibung

start date

Datentyp

date

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

stop date

Datentyp

date

Alias
UMLS CUI [1]
C0806020
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Ähnliche Modelle

Alternate MS Therapy CRFs Multiple Sclerosis Tysabri NCT00027300

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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