ID

25719

Beschrijving

Study ID: 101468/197 Clinical Study ID: SKF-101468/197 Study Title:An open study to compare the PK and tolerability of ropinirole administered as 5 different new formulations with the standard, marketed formulation in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Restless Legs Syndrome

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Versies (1)
  1. 12-09-17 12-09-17 -
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GlaxoSmithKline

Geüploaded op

12 september 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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final examination study completion PK and tolerability of ropinirole as 5 new formulations 101468/197

Engels

final examination study completion PK and tolerability of ropinirole as 5 new formulations 101468/197

1 Formulieren  
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Focus Panel ID
Beschrijving

focus panel

Datatype

integer

Alias
UMLS CUI [1]
C3846158
Patient No
Beschrijving

patient number

Datatype

integer

Alias
UMLS CUI [1]
C1830427
Date
Beschrijving

date

Datatype

date

Alias
UMLS CUI [1]
C0011008
Treatment
Beschrijving

treatment

Datatype

text

Alias
UMLS CUI [1]
C0087111
Study Completion
Beschrijving

Study Completion

Alias
UMLS CUI-1
C0008976
UMLS CUI-2
C0444930
Did the subject complete the study?
Beschrijving

subject completed participation in study

Datatype

text

Alias
UMLS CUI [1]
C2348577
Date of subject completion or discontinuation from the study
Beschrijving

date of subject completed participation in study

Datatype

date

Alias
UMLS CUI [1,1]
C2348577
UMLS CUI [1,2]
C0011008
Time of subject completion or discontinuation from the study
Beschrijving

time of subject completed participation in study

Datatype

time

Alias
UMLS CUI [1,1]
C2348577
UMLS CUI [1,2]
C0040223
Did the subject become pregnant during the study?
Beschrijving

If yes, record details on PREGNANCY NOTIFICATION FORM

Datatype

text

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0008976
Did the subject dicontinue the study prematurely?
Beschrijving

discontinuation of the study

Datatype

boolean

Alias
UMLS CUI [1]
C2348570
If yes, the primary reason for discontinuation
Beschrijving

Record details on NON-SERIOUS ADVERSE EVENTS or SERIOUS ADVERSE EVENT page as appropriate.

Datatype

text

Alias
UMLS CUI [1,1]
C2348570
UMLS CUI [1,2]
C0582550
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Similar models

final examination study completion PK and tolerability of ropinirole as 5 new formulations 101468/197

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
focus panel
Item
Focus Panel ID
integer
C3846158 (UMLS CUI [1])
patient number
Item
Patient No
integer
C1830427 (UMLS CUI [1])
date
Item
Date
date
C0011008 (UMLS CUI [1])
treatment
Item
Treatment
text
C0087111 (UMLS CUI [1])
Item Group
Study Completion
C0008976 (UMLS CUI-1)
C0444930 (UMLS CUI-2)
Item
Did the subject complete the study?
text
C2348577 (UMLS CUI [1])
subject completed participation in study
Code List
Did the subject complete the study?
CL Item
Yes (Yes)
CL Item
No (No)
date of subject completed participation in study
Item
Date of subject completion or discontinuation from the study
date
C2348577 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
time of subject completed participation in study
Item
Time of subject completion or discontinuation from the study
time
C2348577 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Item
Did the subject become pregnant during the study?
text
C0032961 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
pregnancy during study
Code List
Did the subject become pregnant during the study?
CL Item
Not applicable (Not of childbearing potential or male) (Not applicable)
CL Item
Yes (Yes)
CL Item
No (No)
discontinuation of the study
Item
Did the subject dicontinue the study prematurely?
boolean
C2348570 (UMLS CUI [1])
Item
If yes, the primary reason for discontinuation
text
C2348570 (UMLS CUI [1,1])
C0582550 (UMLS CUI [1,2])
reason for premature study termination
Code List
If yes, the primary reason for discontinuation
CL Item
Adverse Event (Adverse Event)
CL Item
Lost to follow up (Lost to follow up)
CL Item
Protocol violation (Protocol violation)
CL Item
Other, specify (Other, specify)
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