ID

27273

Descripción

Study ID: 101468/188 Clinical Study ID: SKF-101468/188 Study Title:A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Parkinson Disease Module: Study Conclusion

Palabras clave

Versiones (1)
  1. 6/11/17 6/11/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

6 de noviembre 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 :

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

GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

Inglés

Study Conclusion

1 formularios  
  1. StudyEvent: ODM
    1. Study Conclusion
Study Conclusion
Descripción

Study Conclusion

Alias
UMLS CUI-1
C2348568
UMLS CUI-2
C1707478
UMLS CUI-3
C0008976
UMLS CUI-4
C0035258
Did the patient complete the study according to the protocol?
Descripción

End of Study

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0444496
If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
Descripción

primary cause of withdrawal

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
Primary cause of withdrawal: If 'Other', please specify
Descripción

primary cause of withdrawal

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
Investigator’s Signature
Descripción

Investigator’s Signature

Tipo de datos

text

Alias
UMLS CUI [1]
C2346576
Investigator’s Signature Date
Descripción

Investigator’s Signature Date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
Volver a la parte superior de la página

Similar models

Study Conclusion

1 formularios
  1. StudyEvent: ODM
    1. Study Conclusion
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Study Conclusion
C2348568 (UMLS CUI-1)
C1707478 (UMLS CUI-2)
C0008976 (UMLS CUI-3)
C0035258 (UMLS CUI-4)
End of Study
Item
Did the patient complete the study according to the protocol?
boolean
C2348568 (UMLS CUI [1,1])
C0444496 (UMLS CUI [1,2])
Item
If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
integer
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
primary cause of withdrawal
Code List
If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
CL Item
Adverse experience (please complete AE page)  (1)
CL Item
Insufficient therapeutic effect (2)
CL Item
Protocol deviation (including non-compliance) (3)
CL Item
Lost to follow-up (4)
CL Item
Other (5)
primary cause of withdrawal
Item
Primary cause of withdrawal: If 'Other', please specify
text
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Investigator’s Signature
Item
Investigator’s Signature
text
C2346576 (UMLS CUI [1])
Investigator’s Signature Date
Item
Investigator’s Signature Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
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