ID

25651

Description

Study ID: 101468/228 Clinical Study ID: 101468/228 Study Title:A two year Phase IIIb randomised, multicenter, double-blind, SINEMET controlled, parallel group, flexible dose study, to assess the effectiveness of controlled release ropinirole add-on therapy to L-dopa at increasing the time to onset of dyskinesia in Parkinson's disease subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363727 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Dyskinesias; Parkinson Disease; Parkinson's Disease Study part: Concomitant medications

Mots-clés

Versions (4)
  1. 11/08/2017 11/08/2017 -
  2. 18/08/2017 18/08/2017 -
  3. 18/08/2017 18/08/2017 -
  4. 08/09/2017 08/09/2017 -
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8 septembre 2017

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Creative Commons BY-NC 3.0
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Concomitant medications GSK study Dyskinesia in Parkinson's disease NCT00363727

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Concomitant medications GSK study Dyskinesia in Parkinson's disease NCT00363727

1 Formulaires  
General information
Description

General information

Protocol identifier
Description

Protocol identifier

Type de données

integer

Alias
UMLS CUI [1]
C2826693
Subject Identifier
Description

Subject Identifier

Type de données

text

Alias
UMLS CUI [1]
C2348585
Visit Description
Description

Visit Description

Type de données

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0678257
Concomitant medications
Description

Concomitant medications

Were any concomitant medications taken by the subject during the study?
Description

If Yes, record each medication on a separate line using Trade Names where possible. If the medication is related to a Non-Serious Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.

Type de données

boolean

Alias
UMLS CUI [1]
C2347852
Drug name
Description

(Trade Name preferred)

Type de données

text

Alias
UMLS CUI [1]
C0013227
Total daily dose
Description

Total daily dose

Type de données

float

Alias
UMLS CUI [1]
C2348070
Units
Description

The following lists of abbreviations are examples which can be used to aid the completion of the appropriate items on the L-Dopa page.These are not all inclusive lists and are for guidance only, other abbreviations may be used if necessary. Abbreviation Label: TAB = Tablet, MCL = Microlitre, ML = Millilitre, L = Litre, MCG = Microgram, MG = Milligram, G = Gram

Type de données

integer

Alias
UMLS CUI [1,1]
C0450442
UMLS CUI [1,2]
C1519795
Route
Description

The following lists of abbreviations are examples which can be used to aid the completion of the appropriate items on the L-Dopa page.These are not all inclusive lists and are for guidance only, other abbreviations may be used if necessary. Abbreviation Label: IM = Intramuscular, IH = Inhalation, IV = Intravenous, NS = Nasal, TP = Topical, PO = Oral, VG = Vaginal

Type de données

integer

Alias
UMLS CUI [1]
C0013153
Reason for Medication
Description

Reason for Medication

Type de données

integer

Alias
UMLS CUI [1]
C2826696
Start Date
Description

Start Date

Type de données

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Stop Date

Type de données

date

Alias
UMLS CUI [1]
C0806020
Ongoing Medication?
Description

Ongoing Medication

Type de données

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Concomitant medications GSK study Dyskinesia in Parkinson's disease NCT00363727

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
General information
Protocol identifier
Item
Protocol identifier
integer
C2826693 (UMLS CUI [1])
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Visit Description
Item
Visit Description
text
C0545082 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Item Group
Concomitant medications
Concomitant medications
Item
Were any concomitant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1])
Drug name
Item
Drug name
text
C0013227 (UMLS CUI [1])
Total daily dose
Item
Total daily dose
float
C2348070 (UMLS CUI [1])
Units
Item
Units
integer
C0450442 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Route
Item
Route
integer
C0013153 (UMLS CUI [1])
Reason for Medication
Item
Reason for Medication
integer
C2826696 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Ongoing Medication
Item
Ongoing Medication?
boolean
C2826666 (UMLS CUI [1])
Retour au début de la page 

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