ID
39424
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 (9)
- 12/10/19 12/10/19 -
- 12/11/19 12/11/19 -
- 12/11/19 12/11/19 -
- 12/11/19 12/11/19 -
- 12/11/19 12/11/19 -
- 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 1; Visit 2; Visit 3; Visit 4; Visit 5; Visit 6; Visit 7; Visit 8; Visit Maintenance 1 +2; Early Withdrawal; Follow up; Optional Visit - Check In
Description
Check-In Review
Alias
- UMLS CUI-1
- C4321547
- UMLS CUI-2
- C0699752
Description
Date of Visit
Data type
date
Alias
- UMLS CUI [1]
- C1320303
Description
Please ensure Concomitant Medication or Non-Drug Therapy record is added/updated as needed.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0443172
- UMLS CUI [2]
- C0033082
Description
Please update the appropriate medical history.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0392747
- UMLS CUI [2]
- C0850624
- UMLS CUI [3]
- C0012634
- UMLS CUI [4]
- C1519384
Description
Please ensure that an Adverse Event with a start date occurring between the previous and current visit dates is entered.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0545082
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1711239
Description
Please ensure SOOS questionnaire form is completed for this visit.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1272517
- UMLS CUI [1,2]
- C0037313
- UMLS CUI [1,3]
- C0034394
- UMLS CUI [1,4]
- C0205197
Description
Please provide a reason
Data type
text
Alias
- UMLS CUI [1]
- C0392360
Description
Did the Investigator review the subject diary?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0035173
- UMLS CUI [1,2]
- C3166277
- UMLS CUI [1,3]
- C3890583
Description
Was investigational product tolerated?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0013220
Description
Will the patient continue in the study?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0805733
- UMLS CUI [1,2]
- C2603343
Description
Optional Visit
Alias
- UMLS CUI-1
- C0545082
- UMLS CUI-2
- C1518600
Description
Optional Visit Number
Data type
integer
Alias
- UMLS CUI [1,1]
- C1549755
- UMLS CUI [1,2]
- C1518600
Similar models
Visit 1; Visit 2; Visit 3; Visit 4; Visit 5; Visit 6; Visit 7; Visit 8; Visit Maintenance 1 +2; Early Withdrawal; Follow up; Optional Visit - Check In
C0443172 (UMLS CUI [1,2])
C0033082 (UMLS CUI [2])
C0392747 (UMLS CUI [1,2])
C0850624 (UMLS CUI [2])
C0012634 (UMLS CUI [3])
C1519384 (UMLS CUI [4])
C0545082 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1711239 (UMLS CUI [1,4])
C0037313 (UMLS CUI [1,2])
C0034394 (UMLS CUI [1,3])
C0205197 (UMLS CUI [1,4])
C3166277 (UMLS CUI [1,2])
C3890583 (UMLS CUI [1,3])
C0013220 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,2])
C1518600 (UMLS CUI [1,2])