ID

20664

Descripción

Documentation Part: Pharmacogenetic (PGx) Research An Open Label, Repeat Dose, Dose Escalation Study Conducted in Parkinson's Disease Patients to Characterize the Pharmacokinetics and Effect of Food on Ropinirole Prolonged Release (PR/CR) 12mg Tablets. ClinicalTrials.gov Identifier: NCT00460148 https://clinicaltrials.gov/ct2/show/NCT00460148?term=NCT00460148&rank=1 Responsible Party: GlaxoSmithKline

Link

https://clinicaltrials.gov/ct2/show/NCT00460148?term=NCT00460148&rank=1

Palabras clave

Versiones (1)
  1. 9/3/17 9/3/17 -
Subido en

9 de marzo de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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Pharmacogenetic (PGx) Research Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

Inglés

Pharmacogenetic (PGx) Research Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

1 formularios  
Subject information
Descripción

Subject information

Alias
UMLS CUI-1
C2707520
Subject identifier
Descripción

Subject identifier

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Consent for PGx Research (DNA)
Descripción

Consent for PGx Research (DNA)

Alias
UMLS CUI-1
C0021430
UMLS CUI-2
C0031325
UMLS CUI-3
C0035168
Has informed consent been obtained for PGx research?
Descripción

Has informed consent been obtained for PGx research?

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0031325
UMLS CUI [1,3]
C0035168
If Yes, record the date informed consent obtained for PGx research
Descripción

If Yes, record the date informed consent obtained for PGx research

Tipo de datos

date

Unidades de medida
  • Day Month Year
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0021430
Day Month Year
Blood sample collection (DNA)
Descripción

Blood sample collection (DNA)

Alias
UMLS CUI-1
C0200345
UMLS CUI-2
C0012854
Has a blood sample been collected for PGx research?
Descripción

Has a blood sample been collected for PGx research?

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0031325
UMLS CUI [1,3]
C0035168
If Yes, record the date sample taken
Descripción

If Yes, record the date sample taken

Tipo de datos

date

Unidades de medida
  • Day Month Year
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0200345
Day Month Year
Withdrawal of consent for PGx (DNA)
Descripción

Withdrawal of consent for PGx (DNA)

Alias
UMLS CUI-1
C2349954
UMLS CUI-2
C0021430
Has subject withdrawn consent for PGx research?
Descripción

Has subject withdrawn consent for PGx research?

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0021430
If Yes, record the date informed consent withdrawn for PGx research
Descripción

If Yes, record the date informed consent withdrawn for PGx research

Tipo de datos

date

Unidades de medida
  • Day Month Year
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0021430
Day Month Year
Blood sample destruction
Descripción

Blood sample destruction

Alias
UMLS CUI-1
C1948029
UMLS CUI-2
C0178913
Has a request been made for blood sample destruction?
Descripción

Has a request been made for blood sample destruction?

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0686900
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C0178913
If Yes, choose one reason:
Descripción

If Yes, choose one reason:

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C0178913
If other, specify:
Descripción

If other, specify:

Tipo de datos

text

Alias
UMLS CUI [1,1]
C2348235
UMLS CUI [1,2]
C0392360
UMLS CUI [1,3]
C1948029
UMLS CUI [1,4]
C0178913
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Similar models

Pharmacogenetic (PGx) Research Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Subject information
C2707520 (UMLS CUI-1)
Subject identifier
Item
Subject identifier
text
C2348585 (UMLS CUI [1])
Item Group
Consent for PGx Research (DNA)
C0021430 (UMLS CUI-1)
C0031325 (UMLS CUI-2)
C0035168 (UMLS CUI-3)
Item
Has informed consent been obtained for PGx research?
text
C0021430 (UMLS CUI [1,1])
C0031325 (UMLS CUI [1,2])
C0035168 (UMLS CUI [1,3])
Have liver chemistry results reached or exceeded protocol-defined investigational product stopping criteria?
Code List
Has informed consent been obtained for PGx research?
CL Item
Yes (Y)
CL Item
No (N)
If Yes, record the date informed consent obtained for PGx research
Item
If Yes, record the date informed consent obtained for PGx research
date
C0011008 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Item Group
Blood sample collection (DNA)
C0200345 (UMLS CUI-1)
C0012854 (UMLS CUI-2)
Item
Has a blood sample been collected for PGx research?
text
C0200345 (UMLS CUI [1,1])
C0031325 (UMLS CUI [1,2])
C0035168 (UMLS CUI [1,3])
Has a blood sample been collected for PGx research?
Code List
Has a blood sample been collected for PGx research?
CL Item
Yes (Y)
CL Item
No (N)
If Yes, record the date sample taken
Item
If Yes, record the date sample taken
date
C0011008 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
Item Group
Withdrawal of consent for PGx (DNA)
C2349954 (UMLS CUI-1)
C0021430 (UMLS CUI-2)
Item
Has subject withdrawn consent for PGx research?
text
C2349954 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Has subject withdrawn consent for PGx research?
Code List
Has subject withdrawn consent for PGx research?
CL Item
Yes (Y)
CL Item
No (N)
If Yes, record the date informed consent withdrawn for PGx research
Item
If Yes, record the date informed consent withdrawn for PGx research
date
C0011008 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
Item Group
Blood sample destruction
C1948029 (UMLS CUI-1)
C0178913 (UMLS CUI-2)
Item
Has a request been made for blood sample destruction?
text
C0686900 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
Has a request been made for blood sample destruction?
Code List
Has a request been made for blood sample destruction?
CL Item
Yes (Y)
CL Item
No (N)
Item
If Yes, choose one reason:
text
C0392360 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
If Yes, choose one reason:
Code List
If Yes, choose one reason:
CL Item
Subject withdrew consent for PGx (3)
CL Item
Screen failure (2)
CL Item
Other (Z)
If other, specify:
Item
If other, specify:
text
C2348235 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,4])
Volver a la parte superior de la página 

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