ID

26386

Description

Study Part: Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2). An open-label, up-titration study to assess the dose proportionality of ropinirole controlled release (CR) and to demonstrate the bioequivalence of ropinirole CR (1 x 8 mg) compared to the ropinirole CR (4 x 2 mg) in Parkinson's Disease patients not receiving other dopaminergic therapies. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Phase: phase 2. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP,Zygara. Study Indication: Parkinson Disease. Study ID: 101468/165. Clinical Study ID: 101468/165

Keywords

Versions (1)
  1. 10/16/17 10/16/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 16, 2017

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2) Ropinirole Parkinson Disease 101468/165

English

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2)

1 forms  
ADVERSE EVENTS & CONCOMITANT MEDICATIONS
Description

ADVERSE EVENTS & CONCOMITANT MEDICATIONS

Alias
UMLS CUI-1
C0877248
UMLS CUI-3
C2347852
Patient Number
Description

Patient Number

Data type

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Description

Centre Number

Data type

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Visit Date
Description

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
Has the subject experienced any Adverse Events?
Description

Adverse Events

Data type

boolean

Alias
UMLS CUI [1]
C0877248
Has the subject taken any Concomitant medications?
Description

Concomitant medications

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Back to the top of the page

Similar models

Adverse Events & Concomitant Medications Week 1 Day 1 (Visit 2)

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
ADVERSE EVENTS & CONCOMITANT MEDICATIONS
C0877248 (UMLS CUI-1)
C2347852 (UMLS CUI-3)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Adverse Events
Item
Has the subject experienced any Adverse Events?
boolean
C0877248 (UMLS CUI [1])
Concomitant medications
Item
Has the subject taken any Concomitant medications?
boolean
C2347852 (UMLS CUI [1])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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