ID

39237

Descrizione

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

  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 -
Titolare del copyright

GlaxoSmithKline

Caricato su

11 dicembre 2019

DOI

Per favore, per richiedere un accesso.

Licenza

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

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

Administration
Descrizione

Administration

Alias
UMLS CUI-1
C1320722
Study Name
Descrizione

Study Name

Tipo di dati

text

Alias
UMLS CUI [1]
C2348560
Subject ID
Descrizione

Subject ID

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Study Site
Descrizione

Study Site

Tipo di dati

text

Alias
UMLS CUI [1]
C2825164
Pregnancy
Descrizione

Pregnancy

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

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

Tipo di dati

boolean

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

Did the subject become pregnant during the study?

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961

Similar models

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

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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])

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