ID

25947

Descripción

PRIOR RLS TREATMENT MEDICATIONS Ropinirole Case Report Form GSK Study ID: 100013 Clinical Study ID: RRL100013 A 12-Week, Double-Blind, Placebo-Controlled, Twice-Daily Dosing Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Requiring Extended Treatment Coverage

Palabras clave

Versiones (1)
  1. 30/9/17 30/9/17 -
Titular de derechos de autor

gsk

Subido en

30 de septiembre de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

  • El más nuevo
  • Más antiguo
  • Popular
  • El más nuevo
    • El más nuevo
    • Más antiguo
    • Popular

Sin comentarios

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

PRIOR RLS TREATMENT MEDICATIONS Ropinirole Case Report Form GSK RRL100013

Inglés

PRIOR RLS TREATMENT MEDICATIONS Ropinirole Case Report Form GSK RRL100013

1 formularios  
RLS CONCOMITANT MEDICATIONS
Descripción

RLS CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C2347852
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
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
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
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
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
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
Drug name
Descripción

Drug name

Tipo de datos

text

Alias
UMLS CUI [1]
C0013227
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
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
Volver a la parte superior de la página

Similar models

PRIOR RLS TREATMENT MEDICATIONS Ropinirole Case Report Form GSK RRL100013

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
RLS CONCOMITANT MEDICATIONS
C2347852 (UMLS CUI-1)
cabergoline
Item
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
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
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
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
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
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
Drug name
text
C0013227 (UMLS CUI [1])
Modified reported term
Item
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
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])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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