ID
39429
Description
Study ID: 111569 Clinical Study ID: 111569 Study Title: A fixed dose, dose-response study for ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01494532 Sponsor: GlaxoSmithKline Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Ropinirole, placebo Study Indication: Parkinson's Disease
Keywords
Versions (4)
- 12/11/19 12/11/19 -
- 12/11/19 12/11/19 -
- 12/16/19 12/16/19 -
- 1/9/20 1/9/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
January 9, 2020
DOI
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License
Creative Commons BY-NC 3.0
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Ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease (NCT01494532)
Visit 8; Maintenance 1 +2; Early Withdrawal; Follow up; Unscheduled - Central Laboratory
Description
Electronically Transferred Lab Data
Alias
- UMLS CUI-1
- C0745590
- UMLS CUI-2
- C1705822
Description
Laboratory Test
Data type
integer
Alias
- UMLS CUI [1]
- C0022885
Description
Sample collection date
Data type
date
Alias
- UMLS CUI [1]
- C1302413
Description
Sample collection time
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0005834
Description
Laboratory Test not done
Data type
integer
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C1272696
Description
Possible Liver Events
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0877248
- UMLS CUI-3
- C0332149
Description
Was there a protocol defined Liver Chemistry Event for the lab samples collected at this visit?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0023884
- UMLS CUI [1,3]
- C0877248
- UMLS CUI [1,4]
- C0005834
- UMLS CUI [1,5]
- C0545082
Similar models
Visit 8; Maintenance 1 +2; Early Withdrawal; Follow up; Unscheduled - Central Laboratory
C1705822 (UMLS CUI-2)
C0005834 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0877248 (UMLS CUI-2)
C0332149 (UMLS CUI-3)
C0023884 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0545082 (UMLS CUI [1,5])