ID

25663

Beschrijving

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.

Trefwoorden

  1. 12-08-17 12-08-17 -
  2. 12-08-17 12-08-17 -
  3. 08-09-17 08-09-17 -
Geüploaded op

8 september 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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Investigational Product GSK study Dyskinesia in Parkinson's disease NCT00363727

Investigational Product study Dyskinesia in Parkinson's disease NCT00363727

General information
Beschrijving

General information

Protocol identifier
Beschrijving

Protocol identifier

Datatype

integer

Alias
UMLS CUI [1]
C2826693
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Visit date
Beschrijving

Visit date

Datatype

date

Alias
UMLS CUI [1]
C1320303
Visit Description
Beschrijving

Visit Description

Datatype

text

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

Investigational product

Investigational Product
Beschrijving

e.g., Bottle A

Datatype

integer

Alias
UMLS CUI [1]
C0304229
Blinded Dose Level
Beschrijving

Blinded Dose Level

Datatype

integer

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

Start Date

Datatype

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Beschrijving

Stop Date

Datatype

date

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

Investigational Product Container Number

Datatype

integer

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

Missings

Datatype

boolean

Alias
UMLS CUI [1]
C0511958
Compliance
Beschrijving

Compliance

Total Number of Tablets Dispensed
Beschrijving

Total Number of Tablets Dispensed

Datatype

integer

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

Total Number of Tablets Returned

Datatype

integer

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

Similar models

Investigational Product study Dyskinesia in Parkinson's disease NCT00363727

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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