ID

26386

Beschrijving

Study Part: Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2). An open-label, up-titration study to assess the dose proportionality of ropinirole controlled release (CR) and to demonstrate the bioequivalence of ropinirole CR (1 x 8 mg) compared to the ropinirole CR (4 x 2 mg) in Parkinson's Disease patients not receiving other dopaminergic therapies. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Phase: phase 2. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP,Zygara. Study Indication: Parkinson Disease. Study ID: 101468/165. Clinical Study ID: 101468/165

Trefwoorden

Versies (1)
  1. 16-10-17 16-10-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

16 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2) Ropinirole Parkinson Disease 101468/165

Engels

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2)

1 Formulieren  
ADVERSE EVENTS & CONCOMITANT MEDICATIONS
Beschrijving

ADVERSE EVENTS & CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C0877248
UMLS CUI-3
C2347852
Patient Number
Beschrijving

Patient Number

Datatype

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Beschrijving

Centre Number

Datatype

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Visit Date
Beschrijving

Visit Date

Datatype

date

Alias
UMLS CUI [1]
C1320303
Has the subject experienced any Adverse Events?
Beschrijving

Adverse Events

Datatype

boolean

Alias
UMLS CUI [1]
C0877248
Has the subject taken any Concomitant medications?
Beschrijving

Concomitant medications

Datatype

boolean

Alias
UMLS CUI [1]
C2347852
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Similar models

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2)

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
ADVERSE EVENTS & CONCOMITANT MEDICATIONS
C0877248 (UMLS CUI-1)
C2347852 (UMLS CUI-3)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Adverse Events
Item
Has the subject experienced any Adverse Events?
boolean
C0877248 (UMLS CUI [1])
Concomitant medications
Item
Has the subject taken any Concomitant medications?
boolean
C2347852 (UMLS CUI [1])
Terug naar het begin van de pagina 

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