ID

24787

Descripción

Study ID: 101468/166 Clinical Study ID: SKF-101468/166 Study Title: A Phase II, randomised, double-blind, active-controlled, dose-escalation study to determine the maximum well-tolerated starting dose of a new formulation of ropinirole in Parkinson's Disease patients not receiving other dopaminergic therapies Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Parkinson Disease

Palabras clave

Versiones (4)
  1. 17/8/17 17/8/17 -
  2. 23/8/17 23/8/17 -
  3. 4/9/17 4/9/17 -
  4. 4/9/17 4/9/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

17 de agosto 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.

laboratory evaluation urinalysis determination of the maximum well-tolerated starting dose of ropinirole in Parkinson's Disease 101468/166

Inglés

laboratory evaluation urinalysis determination of the maximum well-tolerated starting dose of ropinirole in Parkinson's Disease 101468/166

1 formularios  
Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Patient Initials
Descripción

patient's initials

Tipo de datos

text

Alias
UMLS CUI [1]
C2986440
Patient No.
Descripción

patient number

Tipo de datos

integer

Alias
UMLS CUI [1]
C1830427
URINALYSIS
Descripción

URINALYSIS

Alias
UMLS CUI-1
C0042014
URINALYSIS
Descripción

If not "Not Done", record the date of sample taking below.

Tipo de datos

text

Alias
UMLS CUI [1]
C0042014
Date of Sample
Descripción

If not "Not Done" above, fulfill this item.

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0011008
pH
Descripción

pH

Alias
UMLS CUI-1
C0042044
Result
Descripción

Numeric only

Tipo de datos

integer

Alias
UMLS CUI [1]
C1274040
Clin Sig
Descripción

If result is clincally significant, enter a tickmark here. Otherwise leave this field empty.

Tipo de datos

text

Protein
Descripción

Protein

Alias
UMLS CUI-1
C0262923
Result
Descripción

Numeric only

Tipo de datos

integer

Alias
UMLS CUI [1]
C1274040
Clin Sig
Descripción

If result is clincally significant, enter a tickmark here. Otherwise leave this field empty.

Tipo de datos

text

Glucose
Descripción

Glucose

Alias
UMLS CUI-1
C0004076
Result
Descripción

Numeric only

Tipo de datos

integer

Alias
UMLS CUI [1]
C1274040
Clin Sig
Descripción

If result is clincally significant, enter a tickmark here. Otherwise leave this field empty.

Tipo de datos

text

Blood
Descripción

Blood

Alias
UMLS CUI-1
C0018965
Result
Descripción

Numeric only

Tipo de datos

integer

Alias
UMLS CUI [1]
C1274040
Clin Sig
Descripción

If result is clincally significant, enter a tickmark here. Otherwise leave this field empty.

Tipo de datos

text

Bilirubin
Descripción

Bilirubin

Alias
UMLS CUI-1
C0042040
Result
Descripción

Numeric only

Tipo de datos

integer

Alias
UMLS CUI [1]
C1274040
Clin Sig
Descripción

If result is clincally significant, enter a tickmark here. Otherwise leave this field empty.

Tipo de datos

text

Volver a la parte superior de la página

Similar models

laboratory evaluation urinalysis determination of the maximum well-tolerated starting dose of ropinirole in Parkinson's Disease 101468/166

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
patient's initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
patient number
Item
Patient No.
integer
C1830427 (UMLS CUI [1])
Item Group
URINALYSIS
C0042014 (UMLS CUI-1)
Item
URINALYSIS
text
C0042014 (UMLS CUI [1])
hematology
Code List
URINALYSIS
CL Item
Not Done (Not Done)
CL Item
Done (Done)
date of sample
Item
Date of Sample
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
pH
C0042044 (UMLS CUI-1)
result
Item
Result
integer
C1274040 (UMLS CUI [1])
Item
Clin Sig
text
clinically significant
Code List
Clin Sig
CL Item
Clin Sig (Clin Sig)
Item Group
Protein
C0262923 (UMLS CUI-1)
result
Item
Result
integer
C1274040 (UMLS CUI [1])
Item
Clin Sig
text
clinically significant
Code List
Clin Sig
CL Item
Clin Sig (Clin Sig)
Item Group
Glucose
C0004076 (UMLS CUI-1)
result
Item
Result
integer
C1274040 (UMLS CUI [1])
Item
Clin Sig
text
clinically significant
Code List
Clin Sig
CL Item
Clin Sig (Clin Sig)
Item Group
Blood
C0018965 (UMLS CUI-1)
result
Item
Result
integer
C1274040 (UMLS CUI [1])
Item
Clin Sig
text
clinically significant
Code List
Clin Sig
CL Item
Clin Sig (Clin Sig)
Item Group
Bilirubin
C0042040 (UMLS CUI-1)
result
Item
Result
integer
C1274040 (UMLS CUI [1])
Item
Clin Sig
text
clinically significant
Code List
Clin Sig
CL Item
Clin Sig (Clin Sig)
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