ID

25455

Description

Study ID: 101468/166 Clinical Study ID: SKF-101468/166 Study Title: A Phase II, randomised, double-blind, active-controlled, dose-escalation study to determine the maximum well-tolerated starting dose of a new formulation of ropinirole in Parkinson's Disease patients not receiving other dopaminergic therapies Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Parkinson Disease

Keywords

Versions (2)
  1. 8/22/17 8/22/17 -
  2. 9/4/17 9/4/17 -
Uploaded on

September 4, 2017

DOI

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License

Creative Commons BY-NC 3.0
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visit 2 study medication administration starting dose of ropinirole Parkinson's Disease 101468/166

English

visit 2 study medication administration starting dose of ropinirole Parkinson's Disease 101468/166

1 forms  
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Patient Initials
Description

patient's initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Patient No.
Description

patient number

Data type

integer

Alias
UMLS CUI [1]
C1830427
Dose#1
Description

Dose#1

Alias
UMLS CUI-1
C3174092
Date of Administration
Description

date of administration

Data type

date

Alias
UMLS CUI [1,1]
C1533734
UMLS CUI [1,2]
C0011008
Time of Administration
Description

24-hour clock

Data type

time

Alias
UMLS CUI [1]
C1317775
Dose#2
Description

Dose#2

Alias
UMLS CUI-1
C3174092
Time of Administration
Description

24-hour clock

Data type

time

Alias
UMLS CUI [1]
C1317775
Dose#3
Description

Dose#3

Alias
UMLS CUI-1
C3174092
Time of Administration
Description

24-hour clock

Data type

time

Alias
UMLS CUI [1]
C1317775
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Similar models

visit 2 study medication administration starting dose of ropinirole Parkinson's Disease 101468/166

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
patient's initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
patient number
Item
Patient No.
integer
C1830427 (UMLS CUI [1])
Item Group
Dose#1
C3174092 (UMLS CUI-1)
date of administration
Item
Date of Administration
date
C1533734 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
time of administration
Item
Time of Administration
time
C1317775 (UMLS CUI [1])
Item Group
Dose#2
C3174092 (UMLS CUI-1)
time of administration
Item
Time of Administration
time
C1317775 (UMLS CUI [1])
Item Group
Dose#3
C3174092 (UMLS CUI-1)
time of administration
Item
Time of Administration
time
C1317775 (UMLS CUI [1])
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