ID

26109

Beskrivning

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: Concomitant Medication

Nyckelord

Versioner (1)
  1. 2017-10-09 2017-10-09 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

9 oktober 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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Dose strength equivalence of ropinirole CR in healthy adults Concomitant Medication 101468/219

Engelsk

Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

1 Formulär  
Concomitant Medication
Beskrivning

Concomitant Medication

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C0244821
Are there any concomitant medication CHANGES since the start of the study?
Beskrivning

If ’YES’, please record all medications used below. Where appropriate, medical conditions should be recorded on the Adverse Events Form, utilizing the same terminology. If a medication has had a dosage change it must be recorded with the start and stop date.

Datatyp

boolean

Alias
UMLS CUI [1]
C2347852
drug name
Beskrivning

Trade Name Preferred

Datatyp

text

Alias
UMLS CUI [1,1]
C2360065
UMLS CUI [1,2]
C2347852
Single Dose/Unit
Beskrivning

dose per unit

Datatyp

integer

Alias
UMLS CUI [1,1]
C3174092
UMLS CUI [1,2]
C2347852
Frequency of this Dose
Beskrivning

medication frequency

Datatyp

text

Alias
UMLS CUI [1,1]
C3476109
UMLS CUI [1,2]
C2347852
Route
Beskrivning

drug application route

Datatyp

text

Alias
UMLS CUI [1,1]
C0013153
UMLS CUI [1,2]
C2347852
Indication
Beskrivning

medication indication

Datatyp

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C2347852
Duration
Beskrivning

duration of medication

Datatyp

text

Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C2347852
End Date
Beskrivning

end date of medication

Datatyp

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0806020
Continuing at end of study?
Beskrivning

continuing medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
C0244821 (UMLS CUI-2)
concomitant medication
Item
Are there any concomitant medication CHANGES since the start of the study?
boolean
C2347852 (UMLS CUI [1])
drug name
Item
drug name
text
C2360065 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
dose per unit
Item
Single Dose/Unit
integer
C3174092 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
medication frequency
Item
Frequency of this Dose
text
C3476109 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
drug application route
Item
Route
text
C0013153 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
medication indication
Item
Indication
text
C3146298 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
duration of medication
Item
Duration
text
C0449238 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
end date of medication
Item
End Date
date
C2347852 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
continuing medication
Item
Continuing at end of study?
boolean
C2826666 (UMLS CUI [1])
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