ID

25810

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 (2)
  1. 9/20/17 9/20/17 -
  2. 9/20/17 9/20/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 20, 2017

DOI

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License

Creative Commons BY-NC 3.0
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baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

English

baseline eligibility 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
ELIGIBILITY QUESTION
Description

ELIGIBILITY QUESTION

Alias
UMLS CUI-1
C1516637
Did the subject meet all the entry criteria?
Description

If No, ✔ all boxes corresponding to violations of any exclusion criteria. Do not enter the subject into the study if they failed any exclusion criteria below.

Data type

text

Alias
UMLS CUI [1]
C1516637
EXCLUSION CRITERIA
Description

EXCLUSION CRITERIA

Alias
UMLS CUI-1
C0680251
Exclusion Criteria
Description

✔ the box corresponding to any of the exclusion criteria that disqualified the subject from entry.

Data type

integer

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Similar models

baseline eligibility 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])
Item Group
ELIGIBILITY QUESTION
C1516637 (UMLS CUI-1)
Item
Did the subject meet all the entry criteria?
text
C1516637 (UMLS CUI [1])
eligibility criteria
Code List
Did the subject meet all the entry criteria?
CL Item
Yes (Y)
CL Item
No (N)
Item Group
EXCLUSION CRITERIA
C0680251 (UMLS CUI-1)
Item
Exclusion Criteria
integer
exclusion criteria
Code List
Exclusion Criteria
CL Item
Subjects with clinically significant abnormalities in Laboratory or ECG tests at Screening. (1)
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