ID

26113

Beschrijving

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

Trefwoorden

  1. 09-10-17 09-10-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

9 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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

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

Form D
Beschrijving

Form D

Alias
UMLS CUI-1
C0011065
Certified Cause of Death
Beschrijving

Certified Cause of Death

Datatype

text

Alias
UMLS CUI [1]
C0007465
Date of Death
Beschrijving

Date of Death

Datatype

date

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

post-mortem

Datatype

boolean

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

Was a post-mortem carried out?

Datatype

text

Alias
UMLS CUI [1]
C0004398

Similar models

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

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])

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