ID

25663

Description

Study ID: 101468/228 Clinical Study ID: 101468/228 Study Title:A two year Phase IIIb randomised, multicenter, double-blind, SINEMET controlled, parallel group, flexible dose study, to assess the effectiveness of controlled release ropinirole add-on therapy to L-dopa at increasing the time to onset of dyskinesia in Parkinson's disease subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363727 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Dyskinesias; Parkinson Disease; Parkinson's Disease Study part: Investigational Product.

Keywords

Versions (3)
  1. 8/12/17 8/12/17 -
  2. 8/12/17 8/12/17 -
  3. 9/8/17 9/8/17 -
Uploaded on

September 8, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Investigational Product GSK study Dyskinesia in Parkinson's disease NCT00363727

English

Investigational Product study Dyskinesia in Parkinson's disease NCT00363727

1 forms  
General information
Description

General information

Protocol identifier
Description

Protocol identifier

Data type

integer

Alias
UMLS CUI [1]
C2826693
Subject Identifier
Description

Subject Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Visit date
Description

Visit date

Data type

date

Alias
UMLS CUI [1]
C1320303
Visit Description
Description

Visit Description

Data type

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0678257
Investigational product
Description

Investigational product

Investigational Product
Description

e.g., Bottle A

Data type

integer

Alias
UMLS CUI [1]
C0304229
Blinded Dose Level
Description

Blinded Dose Level

Data type

integer

Alias
UMLS CUI [1,1]
C0013072
UMLS CUI [1,2]
C3174092
Start Date
Description

Start Date

Data type

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Stop Date

Data type

date

Alias
UMLS CUI [1]
C0806020
Investigational Product Container Number
Description

Investigational Product Container Number

Data type

integer

Alias
UMLS CUI [1,1]
C3898691
UMLS CUI [1,2]
C0449788
Has the subject missed investigational product for> 3 consecutive days?
Description

Missings

Data type

boolean

Alias
UMLS CUI [1]
C0511958
Compliance
Description

Compliance

Total Number of Tablets Dispensed
Description

Total Number of Tablets Dispensed

Data type

integer

Alias
UMLS CUI [1,1]
C0805077
UMLS CUI [1,2]
C0039225
Total Number of Tablets Returned
Description

Total Number of Tablets Returned

Data type

integer

Alias
UMLS CUI [1,1]
C2699071
UMLS CUI [1,2]
C0039225
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Similar models

Investigational Product study Dyskinesia in Parkinson's disease NCT00363727

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
General information
Protocol identifier
Item
Protocol identifier
integer
C2826693 (UMLS CUI [1])
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Visit date
Item
Visit date
date
C1320303 (UMLS CUI [1])
Visit Description
Item
Visit Description
text
C0545082 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Item Group
Investigational product
Investigational Product
Item
Investigational Product
integer
C0304229 (UMLS CUI [1])
Blinded Dose Level
Item
Blinded Dose Level
integer
C0013072 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Investigational Product Container Number
Item
Investigational Product Container Number
integer
C3898691 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Missings
Item
Has the subject missed investigational product for> 3 consecutive days?
boolean
C0511958 (UMLS CUI [1])
Item Group
Compliance
Total Number of Tablets Dispensed
Item
Total Number of Tablets Dispensed
integer
C0805077 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Total Number of Tablets Returned
Item
Total Number of Tablets Returned
integer
C2699071 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
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