ID

25810

Descripción

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

Palabras clave

  1. 20/9/17 20/9/17 -
  2. 20/9/17 20/9/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

20 de septiembre de 2017

DOI

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Licencia

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
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Descripción

subject number

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
ELIGIBILITY QUESTION
Descripción

ELIGIBILITY QUESTION

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

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.

Tipo de datos

text

Alias
UMLS CUI [1]
C1516637
EXCLUSION CRITERIA
Descripción

EXCLUSION CRITERIA

Alias
UMLS CUI-1
C0680251
Exclusion Criteria
Descripción

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

Tipo de datos

integer

Similar models

baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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