ID

25810

Beskrivning

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

Nyckelord

  1. 2017-09-20 2017-09-20 -
  2. 2017-09-20 2017-09-20 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

20 september 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

Administrative Data
Beskrivning

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Beskrivning

subject number

Datatyp

integer

Alias
UMLS CUI [1]
C2348585
ELIGIBILITY QUESTION
Beskrivning

ELIGIBILITY QUESTION

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

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.

Datatyp

text

Alias
UMLS CUI [1]
C1516637
EXCLUSION CRITERIA
Beskrivning

EXCLUSION CRITERIA

Alias
UMLS CUI-1
C0680251
Exclusion Criteria
Beskrivning

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

Datatyp

integer

Similar models

baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
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
Code List
Exclusion Criteria
CL Item
Subjects with clinically significant abnormalities in Laboratory or ECG tests at Screening. (1)

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