ID

27536

Descripción

Study Part: Study Conclusion Follow- Up (Visit 10). An open-label, up-titration study to assess the dose proportionality of ropinirole controlled release (CR) and to demonstrate the bioequivalence of ropinirole CR (1 x 8 mg) compared to the ropinirole CR (4 x 2 mg) in Parkinson's Disease patients not receiving other dopaminergic therapies. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Phase: phase 2. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP,Zygara. Study Indication: Parkinson Disease. Study ID: 101468/165. Clinical Study ID: 101468/165

Palabras clave

Versiones (1)
  1. 19/11/17 19/11/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

19 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.

Study Conclusion Follow- Up (Visit 10) Ropinirole Parkinson Disease 101468/165

Inglés

Study Conclusion Follow- Up (Visit 10)

1 formularios  
STUDY CONCLUSION
Descripción

STUDY CONCLUSION

Alias
UMLS CUI-1
C1707478
UMLS CUI-2
C0008972
Subject Number
Descripción

Subject Number

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Did the subject complete the study as planned?
Descripción

Study Conclusion

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1707478
UMLS CUI [1,2]
C0008972
If ’NO’, mark the one most appropriate category
Descripción

Study Conclusion

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1707478
UMLS CUI [1,2]
C0008972
Other, Please specify
Descripción

Other

Tipo de datos

text

Alias
UMLS CUI [1]
C0205394
Comments on reason for withdrawal:
Descripción

Comment reason for withdrawal

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0947611
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0392360
UMLS CUI [1,4]
C0008976
Date of Withdrawal:
Descripción

Date of Withdrawal

Tipo de datos

date

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0011008
Time of Withdrawal:
Descripción

Time of Withdrawal

Tipo de datos

time

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0040223
Date of Final Dose:
Descripción

Date of Final Dose

Tipo de datos

date

Alias
UMLS CUI [1]
C1531784
Time of Final Dose:
Descripción

Time of Final Dose

Tipo de datos

time

Alias
UMLS CUI [1]
C0946444
Volver a la parte superior de la página

Similar models

Study Conclusion Follow- Up (Visit 10)

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
STUDY CONCLUSION
C1707478 (UMLS CUI-1)
C0008972 (UMLS CUI-2)
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Study Conclusion
Item
Did the subject complete the study as planned?
boolean
C1707478 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
Item
If ’NO’, mark the one most appropriate category
integer
C1707478 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
Study Conclusion
Code List
If ’NO’, mark the one most appropriate category
CL Item
Adverse Event (complete Adverse Event Form) (1)
C0877248 (UMLS CUI-1)
(Comment:en)
CL Item
Insufficient therapeutic effect (2)
C1527144 (UMLS CUI-1)
(Comment:en)
CL Item
Deviation from Protocol (including non-compliance) (3)
C1321605 (UMLS CUI-1)
(Comment:en)
CL Item
Lost to Follow-Up (4)
C1302313 (UMLS CUI-1)
(Comment:en)
CL Item
Other (5)
C0205394 (UMLS CUI-1)
(Comment:en)
Other
Item
Other, Please specify
text
C0205394 (UMLS CUI [1])
Comment reason for withdrawal
Item
Comments on reason for withdrawal:
text
C0947611 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
Date of Withdrawal
Item
Date of Withdrawal:
date
C2349954 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of Withdrawal
Item
Time of Withdrawal:
time
C2349954 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Date of Final Dose
Item
Date of Final Dose:
date
C1531784 (UMLS CUI [1])
Time of Final Dose
Item
Time of Final Dose:
time
C0946444 (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