ID
25655
Description
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 Study part: UPDRS Part V.
Keywords
Versions (2)
- 8/12/17 8/12/17 -
- 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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UPDRS Part V GSK study Dyskinesia in Parkinson's disease NCT00363727
UPDRS Part V GSK study Dyskinesia in Parkinson's disease NCT00363727
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UPDRS Part V GSK study Dyskinesia in Parkinson's disease NCT00363727
C0678257 (UMLS CUI [1,2])