ID

39428

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

Mots-clés

Versions (7)
  1. 12/11/19 12/11/19 -
  2. 12/11/19 12/11/19 -
  3. 12/11/19 12/11/19 -
  4. 12/11/19 12/11/19 -
  5. 12/16/19 12/16/19 -
  6. 1/9/20 1/9/20 -
  7. 1/9/20 1/9/20 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

January 9, 2020

DOI

Pour une demande vous connecter.

Licence

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)

Anglais

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

1 Formulaires  
Administration
Description

Administration

Alias
UMLS CUI-1
C1320722
Study Name
Description

Study Name

Type de données

text

Alias
UMLS CUI [1]
C2348560
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Study Site
Description

Study Site

Type de données

text

Alias
UMLS CUI [1]
C2825164
Pregnancy
Description

Pregnancy

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

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

Type de données

boolean

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

Did the subject become pregnant during the study?

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
Retour au début de la page

Similar models

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

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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