ID

24583

Descripción

Study part: RLS Concomitant Medications . A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Clinicaltrials.gov Identifier: NCT00355641. Phase: phase 3. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP, Zygara; Zygara, ZIPEREVE, ZEPREVE, Requip Depot, REQUIP, REPREVE, Modutab, ADARTREL. Study Indication : Restless Legs Syndrome. Study ID: 101468/206. Clinical Study ID: 101468/206.

Palabras clave

Versiones (1)
  1. 7/8/17 7/8/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

7 de agosto de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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RLS Concomitant Medications (CM RLS) Ropinirole Restless Legs Syndrom NCT00355641

Inglés

RLS Concomitant Medications

1 formularios  
RLS CONCOMITANT MEDICATIONS
Descripción

RLS CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C2347852
1. Cabergoline. Was drug ever used?
Descripción

cabergoline

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0107994
Start Date:
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
End Date:
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
2. Pergolide. Was drug ever used?
Descripción

Pergolide

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0031007
Start Date:
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
End Date:
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
3. lisuride. Was drug ever used?
Descripción

lisuride

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023863
Start Date:
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
End Date:
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
4.Bromocriptine. Was drug ever used?
Descripción

bromocriptine

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006230
Start Date:
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
End Date:
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
5. Pramipexole. Was drug ever used?
Descripción

pramipexole

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0074710
Start Date:
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
End Date:
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
6. Levodopa
Descripción

Levodopa

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023570
Start Date:
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
End Date:
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
Other RLS Medications
Descripción

Other RLS Medications

Alias
UMLS CUI-1
C2347852
7a. Drug name
Descripción

Drug name

Tipo de datos

text

Alias
UMLS CUI [1]
C0013227
7b. Modified reported term
Descripción

Modified reported term

Tipo de datos

text

Alias
UMLS CUI [1]
C2826819
GSK Drug synonym
Descripción

Drug synonym

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0871468
GSK Drug Collection code
Descripción

Drug Collection code

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1516698
UMLS CUI [1,3]
C0805701
Failed coding
Descripción

Failed coding Concomitant Agent

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0805701
UMLS CUI [1,2]
C0231175
UMLS CUI [1,3]
C2347852
7c. Start Date
Descripción

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
7d. End Date
Descripción

End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
7e. Did the subject respond to treatment?
Descripción

respond to treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150839
7f. Did the subject tolerate treatment?
Descripción

tolerate treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013220
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Similar models

RLS Concomitant Medications

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
RLS CONCOMITANT MEDICATIONS
C2347852 (UMLS CUI-1)
cabergoline
Item
1. Cabergoline. Was drug ever used?
boolean
C0107994 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
Pergolide
Item
2. Pergolide. Was drug ever used?
boolean
C0031007 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
lisuride
Item
3. lisuride. Was drug ever used?
boolean
C0023863 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
bromocriptine
Item
4.Bromocriptine. Was drug ever used?
boolean
C0006230 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
pramipexole
Item
5. Pramipexole. Was drug ever used?
boolean
C0074710 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
Levodopa
Item
6. Levodopa
boolean
C0023570 (UMLS CUI [1])
Start Date
Item
Start Date:
date
C0808070 (UMLS CUI [1])
End Date
Item
End Date:
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
Item Group
Other RLS Medications
C2347852 (UMLS CUI-1)
Drug name
Item
7a. Drug name
text
C0013227 (UMLS CUI [1])
Modified reported term
Item
7b. Modified reported term
text
C2826819 (UMLS CUI [1])
Drug synonym
Item
GSK Drug synonym
text
C0013227 (UMLS CUI [1,1])
C0871468 (UMLS CUI [1,2])
Drug Collection code
Item
GSK Drug Collection code
text
C0013227 (UMLS CUI [1,1])
C1516698 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Failed coding Concomitant Agent
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,3])
Start Date
Item
7c. Start Date
date
C0808070 (UMLS CUI [1])
End Date
Item
7d. End Date
date
C0806020 (UMLS CUI [1])
respond to treatment
Item
7e. Did the subject respond to treatment?
boolean
C0150839 (UMLS CUI [1])
tolerate treatment
Item
7f. Did the subject tolerate treatment?
boolean
C0013220 (UMLS CUI [1])
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