ID

20655

Beschrijving

Documentation Part: Down-Titration Day 38-44 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

Trefwoorden

Versies (1)
  1. 08-03-17 08-03-17 -
Geüploaded op

8 maart 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Down-Titration Day 38-44 Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

Engels

Down-Titration Day 38-44 Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

1 Formulieren  
Subject information
Beschrijving

Subject information

Alias
UMLS CUI-1
C2707520
Subject identifier
Beschrijving

Subject identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Visit date
Beschrijving

Visit date

Alias
UMLS CUI-1
C1320303
Visit date
Beschrijving

Visit date

Datatype

date

Maateenheden
  • Day Month Year
Alias
UMLS CUI [1]
C1320303
Day Month Year
Investigational Product
Beschrijving

Investigational Product

Alias
UMLS CUI-1
C0304229
Planned timepoint
Beschrijving

Planned timepoint

Datatype

text

Alias
UMLS CUI [1]
C2348792
Date of dose
Beschrijving

Date of dose

Datatype

date

Maateenheden
  • Day Month Year
Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0011008
Day Month Year
Time of dose
Beschrijving

Time of dose

Datatype

time

Maateenheden
  • Hr : Min
Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0040223
Hr : Min
Treatment Confirmation
Beschrijving

Treatment Confirmation

Alias
UMLS CUI-1
C0750484
UMLS CUI-2
C0087111
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Beschrijving

Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?

Datatype

text

Alias
UMLS CUI [1,1]
C0750484
UMLS CUI [1,2]
C0087111
If No, record reason(s)
Beschrijving

If No, record reason(s)

Datatype

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0750484
UMLS CUI [1,3]
C0087111
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Similar models

Down-Titration Day 38-44 Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Subject information
C2707520 (UMLS CUI-1)
Subject identifier
Item
Subject identifier
text
C2348585 (UMLS CUI [1])
Item Group
Visit date
C1320303 (UMLS CUI-1)
Visit date
Item
Visit date
date
C1320303 (UMLS CUI [1])
Item Group
Investigational Product
C0304229 (UMLS CUI-1)
Item
Planned timepoint
text
C2348792 (UMLS CUI [1])
Planned timepoint
Code List
Planned timepoint
CL Item
Day 38 (1)
CL Item
Day 39 (2)
CL Item
Day 40 (3)
CL Item
Day 41 (4)
CL Item
Day 42 (5)
CL Item
Day 43 (6)
Date of dose
Item
Date of dose
date
C0013227 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of dose
Item
Time of dose
time
C0013227 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Item Group
Treatment Confirmation
C0750484 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
text
C0750484 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Code List
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
CL Item
No (N)
CL Item
Yes (Y)
If No, record reason(s)
Item
If No, record reason(s)
text
C0392360 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
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