ID

26110

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: Prior Medication

Trefwoorden

Versies (1)
  1. 09-10-17 09-10-17 -
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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 Prior Medication 101468/219

Engels

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

1 Formulieren  
Prior Medication
Beschrijving

Prior Medication

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C2826257
UMLS CUI-3
C0244821
Has the subject taken any medication within 1 week PRIOR to the first dose of study medication?
Beschrijving

If ’YES’, please record the medications below. NB: Any medications Metabolised by CYPIA2 must be kept constant throughout the study.

Datatype

boolean

Alias
UMLS CUI [1]
C0013227
drug name
Beschrijving

Trade Name Preferred

Datatype

text

Alias
UMLS CUI [1]
C2360065
Single Dose/Unit
Beschrijving

dose per unit

Datatype

integer

Alias
UMLS CUI [1]
C3174092
Frequency of this Dose
Beschrijving

medication frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
Route
Beschrijving

drug application route

Datatype

text

Alias
UMLS CUI [1]
C0013153
Indication
Beschrijving

medication indication

Datatype

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0013227
Duration
Beschrijving

duration of medication

Datatype

text

Alias
UMLS CUI [1,1]
C0449238
UMLS CUI [1,2]
C0013227
End Date
Beschrijving

end date of medication

Datatype

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Continuing at end of study?
Beschrijving

continuing medication

Datatype

boolean

Alias
UMLS CUI [1,1]
C2826666
UMLS CUI [1,2]
C0013227
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Similar models

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

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Prior Medication
C0013227 (UMLS CUI-1)
C2826257 (UMLS CUI-2)
C0244821 (UMLS CUI-3)
medication
Item
Has the subject taken any medication within 1 week PRIOR to the first dose of study medication?
boolean
C0013227 (UMLS CUI [1])
drug name
Item
drug name
text
C2360065 (UMLS CUI [1])
dose per unit
Item
Single Dose/Unit
integer
C3174092 (UMLS CUI [1])
medication frequency
Item
Frequency of this Dose
text
C3476109 (UMLS CUI [1])
drug application route
Item
Route
text
C0013153 (UMLS CUI [1])
medication indication
Item
Indication
text
C3146298 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
duration of medication
Item
Duration
text
C0449238 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
end date of medication
Item
End Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
continuing medication
Item
Continuing at end of study?
boolean
C2826666 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
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