ID

39237

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

11 december 2019

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease

Engelsk

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

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial