ID

25721

Description

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

Keywords

  1. 9/12/17 9/12/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 12, 2017

DOI

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License

Creative Commons BY-NC 3.0

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missing data PK and tolerability of ropinirole as 5 new formulations 101468/197

missing data PK and tolerability of ropinirole as 5 new formulations 101468/197

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Focus Panel ID
Description

focus panel

Data type

integer

Alias
UMLS CUI [1]
C3846158
Patient No
Description

patient number

Data type

integer

Alias
UMLS CUI [1]
C1830427
Treatment
Description

treatment

Data type

text

Alias
UMLS CUI [1]
C0087111
Missing Data
Description

Missing Data

Alias
UMLS CUI-1
C0814891
Form
Description

report form

Data type

text

Alias
UMLS CUI [1]
C1516308
Study day
Description

study day

Data type

integer

Alias
UMLS CUI [1]
C2826182
Missing Data Point
Description

missing data point

Data type

text

Alias
UMLS CUI [1]
C0814891
Reason
Description

reason

Data type

text

Alias
UMLS CUI [1]
C0582550
Initials
Description

initials

Data type

text

Alias
UMLS CUI [1]
C2986440

Similar models

missing data PK and tolerability of ropinirole as 5 new formulations 101468/197

Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
treatment
Item
Treatment
text
C0087111 (UMLS CUI [1])
Item Group
Missing Data
C0814891 (UMLS CUI-1)
report form
Item
Form
text
C1516308 (UMLS CUI [1])
study day
Item
Study day
integer
C2826182 (UMLS CUI [1])
missing data point
Item
Missing Data Point
text
C0814891 (UMLS CUI [1])
reason
Item
Reason
text
C0582550 (UMLS CUI [1])
initials
Item
Initials
text
C2986440 (UMLS CUI [1])

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