ID

26451

Description

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

Keywords

Versions (1)
  1. 10/17/17 10/17/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 17, 2017

DOI

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License

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

English

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

1 forms  
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Description

subject number

Data type

integer

Alias
UMLS CUI [1]
C2348585
RANDOMISATION NUMBER
Description

randomisation number

Data type

integer

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

INVESTIGATIONAL PRODUCT

Alias
UMLS CUI-1
C0304229
Investigational Product
Description

investigational product

Data type

text

Alias
UMLS CUI [1]
C0304229
Blinded Dose Level
Description

medication dosage

Data type

integer

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

start date

Data type

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

stop date

Data type

date

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

investigational product container number

Data type

integer

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

COMPLIANCE

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

total number of tablets dispensed

Data type

integer

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

total number of tablets returned

Data type

integer

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

investigational product compliance

Data type

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C1321605
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Similar models

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

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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