ID

21142

Beschrijving

Documentation Part: Treatment Phase Day 29 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 (2)
  1. 08-03-17 08-03-17 -
  2. 11-04-17 11-04-17 -
Geüploaded op

11 april 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Treatment Phase Day 29 Parkinson's Disease Patient Study On Absorption, Distribution, Metabolism And Excretion Of Ropinirole NCT00460148

Engels

Treatment Phase Day 29 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
Vital signs
Beschrijving

Vital signs

Alias
UMLS CUI-1
C0518766
Date
Beschrijving

Date

Datatype

date

Maateenheden
  • Day Month Year
Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0011008
Day Month Year
Planned Relative Time
Beschrijving

Planned Relative Time

Datatype

text

Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0439564
Planned Absolute time
Beschrijving

Planned Absolute time

Datatype

integer

Maateenheden
  • min
Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C1552097
min
Actual time
Beschrijving

Actual time

Datatype

time

Maateenheden
  • Hr : Min
Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0040223
Hr : Min
Systolic Blood Pressure
Beschrijving

Systolic Blood Pressure

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0871470
mmHg
Diastolic Blood Pressure
Beschrijving

Diastolic Blood Pressure

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0428883
mmHg
Subject position
Beschrijving

Subject position

Datatype

text

Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C1262869
Heart Rate
Beschrijving

Heart Rate

Datatype

integer

Maateenheden
  • beats/min
Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0018810
beats/min
12-Lead-ECG
Beschrijving

12-Lead-ECG

Alias
UMLS CUI-1
C0430456
Start date of ECG
Beschrijving

Start date of ECG

Datatype

date

Maateenheden
  • Day Month Year
Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0013798
Day Month Year
Planned Relative Time
Beschrijving

Planned Relative Time

Datatype

text

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0439564
Start Time of ECG
Beschrijving

Start Time of ECG

Datatype

time

Maateenheden
  • Hr : Min
Alias
UMLS CUI [1,1]
C1301880
UMLS CUI [1,2]
C0013798
Hr : Min
Ventricular Rate
Beschrijving

Ventricular Rate

Datatype

integer

Maateenheden
  • Beats/min
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C2189285
Beats/min
PR Interval
Beschrijving

PR Interval

Datatype

integer

Maateenheden
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429087
msec
QRS Duration
Beschrijving

QRS Duration

Datatype

integer

Maateenheden
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429025
msec
Uncorrected QT Interval
Beschrijving

Uncorrected QT Interval

Datatype

integer

Maateenheden
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1287082
msec
QTc Invertal
Beschrijving

QTc Invertal

Datatype

integer

Maateenheden
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0860814
msec
Result of the ECG
Beschrijving

Enter code for result from the following list: 1=Normal 2=Abnormal - not clinically significant 3=Abnormal - clinically significant 4=No result (not available)

Datatype

integer

Alias
UMLS CUI [1]
C0438154
Invesatigational product
Beschrijving

Invesatigational product

Alias
UMLS CUI-1
C3898691
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
Ambulatory blood pressure monitoring
Beschrijving

Ambulatory blood pressure monitoring

Alias
UMLS CUI-1
C0026426
UMLS CUI-2
C0439841
Start date
Beschrijving

Start date

Datatype

date

Maateenheden
  • Day Month Year
Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0026426
UMLS CUI [1,3]
C0439841
Day Month Year
Start time
Beschrijving

Start time

Datatype

time

Maateenheden
  • Hr : Min
Alias
UMLS CUI [1,1]
C1301880
UMLS CUI [1,2]
C0026426
UMLS CUI [1,3]
C0439841
Hr : Min
Stop time
Beschrijving

Stop time

Datatype

time

Alias
UMLS CUI [1,1]
C1522314
UMLS CUI [1,2]
C0026426
UMLS CUI [1,3]
C0439841
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Similar models

Treatment Phase Day 29 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
Vital signs
C0518766 (UMLS CUI-1)
Date
Item
Date
date
C0518766 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Planned Relative Time
text
C0518766 (UMLS CUI [1,1])
C0439564 (UMLS CUI [1,2])
Planned relative Time
Code List
Planned Relative Time
CL Item
Pre-dose (1)
CL Item
Unscheduled (2)
Planned Absolute time
Item
Planned Absolute time
integer
C0518766 (UMLS CUI [1,1])
C1552097 (UMLS CUI [1,2])
Actual time
Item
Actual time
time
C0518766 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Systolic Blood Pressure
Item
Systolic Blood Pressure
integer
C0518766 (UMLS CUI [1,1])
C0871470 (UMLS CUI [1,2])
Diastolic Blood Pressure
Item
Diastolic Blood Pressure
integer
C0518766 (UMLS CUI [1,1])
C0428883 (UMLS CUI [1,2])
Item
Subject position
text
C0518766 (UMLS CUI [1,1])
C1262869 (UMLS CUI [1,2])
Subject position
Code List
Subject position
CL Item
Supine (1)
CL Item
Standing (3)
Heart Rate
Item
Heart Rate
integer
C0518766 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
Item Group
12-Lead-ECG
C0430456 (UMLS CUI-1)
Start date of ECG
Item
Start date of ECG
date
C0808070 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
Item
Planned Relative Time
text
C0430456 (UMLS CUI [1,1])
C0439564 (UMLS CUI [1,2])
Planned Relative Time
Code List
Planned Relative Time
CL Item
Pre-dose (1)
CL Item
Unscheduled (2)
Start Time of ECG
Item
Start Time of ECG
time
C1301880 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
Ventricular Rate
Item
Ventricular Rate
integer
C0430456 (UMLS CUI [1,1])
C2189285 (UMLS CUI [1,2])
PR Interval
Item
PR Interval
integer
C0430456 (UMLS CUI [1,1])
C0429087 (UMLS CUI [1,2])
QRS Duration
Item
QRS Duration
integer
C0430456 (UMLS CUI [1,1])
C0429025 (UMLS CUI [1,2])
Uncorrected QT Interval
Item
Uncorrected QT Interval
integer
C0430456 (UMLS CUI [1,1])
C1287082 (UMLS CUI [1,2])
QTc Invertal
Item
QTc Invertal
integer
C0430456 (UMLS CUI [1,1])
C0860814 (UMLS CUI [1,2])
Result of the ECG
Item
Result of the ECG
integer
C0438154 (UMLS CUI [1])
Item Group
Invesatigational product
C3898691 (UMLS CUI-1)
Planned timepoint
Item
Planned timepoint
text
C2348792 (UMLS CUI [1])
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
Yes (Y)
CL Item
No (N)
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])
Item Group
Ambulatory blood pressure monitoring
C0026426 (UMLS CUI-1)
C0439841 (UMLS CUI-2)
Start date
Item
Start date
date
C0808070 (UMLS CUI [1,1])
C0026426 (UMLS CUI [1,2])
C0439841 (UMLS CUI [1,3])
Start time
Item
Start time
time
C1301880 (UMLS CUI [1,1])
C0026426 (UMLS CUI [1,2])
C0439841 (UMLS CUI [1,3])
Stop time
Item
Stop time
time
C1522314 (UMLS CUI [1,1])
C0026426 (UMLS CUI [1,2])
C0439841 (UMLS CUI [1,3])
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