ID

25651

Descrizione

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

Keywords

  1. 11/08/17 11/08/17 -
  2. 18/08/17 18/08/17 -
  3. 18/08/17 18/08/17 -
  4. 08/09/17 08/09/17 -
Caricato su

8 settembre 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Concomitant medications GSK study Dyskinesia in Parkinson's disease NCT00363727

Concomitant medications GSK study Dyskinesia in Parkinson's disease NCT00363727

General information
Descrizione

General information

Protocol identifier
Descrizione

Protocol identifier

Tipo di dati

integer

Alias
UMLS CUI [1]
C2826693
Subject Identifier
Descrizione

Subject Identifier

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Visit Description
Descrizione

Visit Description

Tipo di dati

text

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

Concomitant medications

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

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.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2347852
Drug name
Descrizione

(Trade Name preferred)

Tipo di dati

text

Alias
UMLS CUI [1]
C0013227
Total daily dose
Descrizione

Total daily dose

Tipo di dati

float

Alias
UMLS CUI [1]
C2348070
Units
Descrizione

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

Tipo di dati

integer

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

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

Tipo di dati

integer

Alias
UMLS CUI [1]
C0013153
Reason for Medication
Descrizione

Reason for Medication

Tipo di dati

integer

Alias
UMLS CUI [1]
C2826696
Start Date
Descrizione

Start Date

Tipo di dati

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Descrizione

Stop Date

Tipo di dati

date

Alias
UMLS CUI [1]
C0806020
Ongoing Medication?
Descrizione

Ongoing Medication

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2826666

Similar models

Concomitant medications GSK study Dyskinesia in Parkinson's disease NCT00363727

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

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

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