ID

39236

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 (4)
  1. 11/12/2019 11/12/2019 -
  2. 11/12/2019 11/12/2019 -
  3. 16/12/2019 16/12/2019 -
  4. 09/01/2020 09/01/2020 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

11 décembre 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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

Anglais

Visit 8; Maintenance 1 +2; Early Withdrawal; Follow up - Central Laboratory

1 Formulaires  
Administrative
Description

Administrative

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
Electronically Transferred Lab Data
Description

Electronically Transferred Lab Data

Alias
UMLS CUI-1
C0745590
UMLS CUI-2
C1705822
Laboratory Test
Description

Laboratory Test

Type de données

integer

Alias
UMLS CUI [1]
C0022885
Sample collection date
Description

Sample collection date

Type de données

date

Alias
UMLS CUI [1]
C1302413
Sample collection time
Description

Sample collection time

Type de données

time

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0005834
Laboratory Test not done
Description

Laboratory Test not done

Type de données

integer

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C1272696
Possible Liver Events
Description

Possible Liver Events

Alias
UMLS CUI-1
C0023884
UMLS CUI-2
C0877248
UMLS CUI-3
C0332149
Was there a protocol defined Liver Chemistry Event for the lab samples collected at this visit?
Description

Was there a protocol defined Liver Chemistry Event for the lab samples collected at this visit?

Type de données

boolean

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0023884
UMLS CUI [1,3]
C0877248
UMLS CUI [1,4]
C0005834
UMLS CUI [1,5]
C0545082
Retour au début de la page

Similar models

Visit 8; Maintenance 1 +2; Early Withdrawal; Follow up - Central Laboratory

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative
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
Electronically Transferred Lab Data
C0745590 (UMLS CUI-1)
C1705822 (UMLS CUI-2)
Item
Laboratory Test
integer
C0022885 (UMLS CUI [1])
Laboratory Test
Code List
Laboratory Test
CL Item
Haematology  (1)
CL Item
Clinical Chemistry  (2)
CL Item
Urinalysis (3)
Sample collection date
Item
Sample collection date
date
C1302413 (UMLS CUI [1])
Sample collection time
Item
Sample collection time
time
C0040223 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
Item
Laboratory Test not done
integer
C0022885 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Laboratory Test not done
Code List
Laboratory Test not done
CL Item
Not done (1)
Item Group
Possible Liver Events
C0023884 (UMLS CUI-1)
C0877248 (UMLS CUI-2)
C0332149 (UMLS CUI-3)
Was there a protocol defined Liver Chemistry Event for the lab samples collected at this visit?
Item
Was there a protocol defined Liver Chemistry Event for the lab samples collected at this visit?
boolean
C0008000 (UMLS CUI [1,1])
C0023884 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0545082 (UMLS CUI [1,5])
Retour au début de la page 

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