ID

39237

Beschrijving

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

Trefwoorden

Versies (7)
  1. 11-12-19 11-12-19 -
  2. 11-12-19 11-12-19 -
  3. 11-12-19 11-12-19 -
  4. 11-12-19 11-12-19 -
  5. 16-12-19 16-12-19 -
  6. 09-01-20 09-01-20 -
  7. 09-01-20 09-01-20 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

11 december 2019

DOI

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Licentie

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

Engels

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

1 Formulieren  
Administration
Beschrijving

Administration

Alias
UMLS CUI-1
C1320722
Study Name
Beschrijving

Study Name

Datatype

text

Alias
UMLS CUI [1]
C2348560
Subject ID
Beschrijving

Subject ID

Datatype

text

Alias
UMLS CUI [1]
C2348585
Study Site
Beschrijving

Study Site

Datatype

text

Alias
UMLS CUI [1]
C2825164
Pregnancy
Beschrijving

Pregnancy

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

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

Datatype

boolean

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

Did the subject become pregnant during the study?

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
Terug naar het begin van de pagina

Similar models

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

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

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