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
Versies (3)
- 12-08-17 12-08-17 -
- 12-08-17 12-08-17 -
- 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
Beschrijving
Investigational product
Beschrijving
e.g., Bottle A
Datatype
integer
Alias
- UMLS CUI [1]
- C0304229
Beschrijving
Blinded Dose Level
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0013072
- UMLS CUI [1,2]
- C3174092
Beschrijving
Start Date
Datatype
date
Alias
- UMLS CUI [1]
- C0808070
Beschrijving
Stop Date
Datatype
date
Alias
- UMLS CUI [1]
- C0806020
Beschrijving
Investigational Product Container Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3898691
- UMLS CUI [1,2]
- C0449788
Beschrijving
Missings
Datatype
boolean
Alias
- UMLS CUI [1]
- C0511958
Beschrijving
Compliance
Beschrijving
Total Number of Tablets Dispensed
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0805077
- UMLS CUI [1,2]
- C0039225
Beschrijving
Total Number of Tablets Returned
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2699071
- UMLS CUI [1,2]
- C0039225
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Investigational Product study Dyskinesia in Parkinson's disease NCT00363727
C0678257 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])