ID

26113

Description

Study ID: 101468/219 Clinical Study ID: 101468/219 Study Title:An open label, randomised, five-way crossover single-dose pharmacokinetic study to assess dosage strength equivalence of ropinirole CR in healthy male and female volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Parkinson Disease Documentation part: Form D

Keywords

Versions (1)
  1. 10/9/17 10/9/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 9, 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 :

  • Newest
  • Oldest
  • Popular
  • Newest
    • Newest
    • Oldest
    • Popular

No comments

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

Dose strength equivalence of ropinirole CR in healthy adults Form D 101468/219

English

Form D Dose strength equivalence of ropinirole CR in healthy adults 101468/219

1 forms  
Form D
Description

Form D

Alias
UMLS CUI-1
C0011065
Certified Cause of Death
Description

Certified Cause of Death

Data type

text

Alias
UMLS CUI [1]
C0007465
Date of Death
Description

Date of Death

Data type

date

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C0011008
Was a post-mortem carried out?
Description

post-mortem

Data type

boolean

Alias
UMLS CUI [1]
C0004398
If Yes, please summarize findings (include diagnosis):
Description

Was a post-mortem carried out?

Data type

text

Alias
UMLS CUI [1]
C0004398
Back to the top of the page

Similar models

Form D Dose strength equivalence of ropinirole CR in healthy adults 101468/219

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Form D
C0011065 (UMLS CUI-1)
Certified Cause of Death
Item
Certified Cause of Death
text
C0007465 (UMLS CUI [1])
Date of Death
Item
Date of Death
date
C0011065 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
post-mortem
Item
Was a post-mortem carried out?
boolean
C0004398 (UMLS CUI [1])
post-mortem
Item
If Yes, please summarize findings (include diagnosis):
text
C0004398 (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