ID

25810

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

  1. 20-09-17 20-09-17 -
  2. 20-09-17 20-09-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

20 september 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Beschrijving

subject number

Datatype

integer

Alias
UMLS CUI [1]
C2348585
ELIGIBILITY QUESTION
Beschrijving

ELIGIBILITY QUESTION

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

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.

Datatype

text

Alias
UMLS CUI [1]
C1516637
EXCLUSION CRITERIA
Beschrijving

EXCLUSION CRITERIA

Alias
UMLS CUI-1
C0680251
Exclusion Criteria
Beschrijving

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

Datatype

integer

Similar models

baseline eligibility Ropinirole CR Ropinirole IR Monotherapy 101468/168

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])
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)

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial