ID

39428

Beskrivning

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

Nyckelord

Versioner (7)
  1. 2019-12-11 2019-12-11 -
  2. 2019-12-11 2019-12-11 -
  3. 2019-12-11 2019-12-11 -
  4. 2019-12-11 2019-12-11 -
  5. 2019-12-16 2019-12-16 -
  6. 2020-01-09 2020-01-09 -
  7. 2020-01-09 2020-01-09 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

9 januari 2020

DOI

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Licens

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)

Engelsk

Visit 4; Visit 6: Visit 8; Maintenance 2; Early Withdrawal; Follow up; Unscheduled - Pregnancy

1 Formulär  
Administration
Beskrivning

Administration

Alias
UMLS CUI-1
C1320722
Study Name
Beskrivning

Study Name

Datatyp

text

Alias
UMLS CUI [1]
C2348560
Subject ID
Beskrivning

Subject ID

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Study Site
Beskrivning

Study Site

Datatyp

text

Alias
UMLS CUI [1]
C2825164
Pregnancy
Beskrivning

Pregnancy

Alias
UMLS CUI-1
C0032961
Did a female partner of a male subject become pregnant during the study?
Beskrivning

Did a female partner of a male subject become pregnant during the study?

Datatyp

boolean

Alias
UMLS CUI [1]
C0919624
Did the subject become pregnant during the study?
Beskrivning

Did the subject become pregnant during the study?

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
Tillbaka till toppen

Similar models

Visit 4; Visit 6: Visit 8; Maintenance 2; Early Withdrawal; Follow up; Unscheduled - Pregnancy

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administration
C1320722 (UMLS CUI-1)
Study Name
Item
Study Name
text
C2348560 (UMLS CUI [1])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Study Site
Item
Study Site
text
C2825164 (UMLS CUI [1])
Item Group
Pregnancy
C0032961 (UMLS CUI-1)
Did a female partner of a male subject become pregnant during the study?
Item
Did a female partner of a male subject become pregnant during the study?
boolean
C0919624 (UMLS CUI [1])
Did the subject become pregnant during the study?
Item
Did the subject become pregnant during the study?
boolean
C0032961 (UMLS CUI [1])
Tillbaka till toppen 

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