ID

26451

Beschrijving

Study ID: 101468/168 Clinical Study ID: 101468/168 Study Title: A Randomised, Double Blind, Three Period, Cross-Over Study of Ropinirole CR and Ropinirole IR Monotherapy Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara Study Indication: Parkinson Disease

Trefwoorden

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

GlaxoSmithKline

Geüploaded op

17 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Unscheduled visit 2 compliance Ropinirole CR Ropinirole IR Monotherapy 101468/168

Engels

Unscheduled visit 2 compliance Ropinirole CR Ropinirole IR Monotherapy 101468/168

1 Formulieren  
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Beschrijving

subject number

Datatype

integer

Alias
UMLS CUI [1]
C2348585
RANDOMISATION NUMBER
Beschrijving

randomisation number

Datatype

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
INVESTIGATIONAL PRODUCT
Beschrijving

INVESTIGATIONAL PRODUCT

Alias
UMLS CUI-1
C0304229
Investigational Product
Beschrijving

investigational product

Datatype

text

Alias
UMLS CUI [1]
C0304229
Blinded Dose Level
Beschrijving

medication dosage

Datatype

integer

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0304229
Start Date
Beschrijving

start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1]
C0806020
Investigational product Container Number
Beschrijving

investigational product container number

Datatype

integer

Alias
UMLS CUI [1,1]
C3898691
UMLS CUI [1,2]
C0449788
COMPLIANCE
Beschrijving

COMPLIANCE

Alias
UMLS CUI-1
C1321605
Total Number of Tablets Dispensed
Beschrijving

total number of tablets dispensed

Datatype

integer

Alias
UMLS CUI [1,1]
C0805077
UMLS CUI [1,2]
C0039225
Total Number of Tablets Returned
Beschrijving

total number of tablets returned

Datatype

integer

Alias
UMLS CUI [1,1]
C2699071
UMLS CUI [1,2]
C0039225
Has the subject missed investigational product for > 3 consecutive days?
Beschrijving

investigational product compliance

Datatype

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C1321605
Terug naar het begin van de pagina

Similar models

Unscheduled visit 2 compliance Ropinirole CR Ropinirole IR Monotherapy 101468/168

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
subject number
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
randomisation number
Item
RANDOMISATION NUMBER
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Item Group
INVESTIGATIONAL PRODUCT
C0304229 (UMLS CUI-1)
Item
Investigational Product
text
C0304229 (UMLS CUI [1])
investigational product
Code List
Investigational Product
CL Item
Bottle A (Bottle A)
CL Item
Bottle B (Bottle B)
medication dosage
Item
Blinded Dose Level
integer
C0178602 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
start date
Item
Start Date
date
C0808070 (UMLS CUI [1])
stop date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
investigational product container number
Item
Investigational product Container Number
integer
C3898691 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Item Group
COMPLIANCE
C1321605 (UMLS CUI-1)
total number of tablets dispensed
Item
Total Number of Tablets Dispensed
integer
C0805077 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
total number of tablets returned
Item
Total Number of Tablets Returned
integer
C2699071 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Item
Has the subject missed investigational product for > 3 consecutive days?
text
C0304229 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
investigational product compliance
Code List
Has the subject missed investigational product for > 3 consecutive days?
CL Item
Yes (Y)
CL Item
No (N)
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