ID

26744

Beskrivning

Study Part: Dosing Details Week 4 PK Visit (Visit 8). 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

Nyckelord

  1. 2017-10-23 2017-10-23 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

23 oktober 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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Dosing Details Week 4 PK Visit (Visit 8) Ropinirole Parkinson Disease 101468/165

Dosing Details Week 4 PK Visit (Visit 8)

DOSING DETAILS
Beskrivning

DOSING DETAILS

Alias
UMLS CUI-1
C0678766
Dosage given:
Beskrivning

Dosage given:___________ Tablet x ___________ mg

Datatyp

text

Alias
UMLS CUI [1]
C0178602
Date and time of dosing:
Beskrivning

Date and time of dosing

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Dose checked and administered by:
Beskrivning

dose administered by

Datatyp

text

Alias
UMLS CUI [1]
C2348343
Dose checked and witnessed by:
Beskrivning

Dose checked and witnessed by

Datatyp

text

Alias
UMLS CUI [1,1]
C0682356
UMLS CUI [1,2]
C1283174
UMLS CUI [1,3]
C0178602
Comments:
Beskrivning

Comments

Datatyp

text

Alias
UMLS CUI [1]
C0947611

Similar models

Dosing Details Week 4 PK Visit (Visit 8)

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
DOSING DETAILS
C0678766 (UMLS CUI-1)
Dosage
Item
Dosage given:
text
C0178602 (UMLS CUI [1])
Date and time of dosing
Item
Date and time of dosing:
datetime
C0013227 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
dose administered by
Item
Dose checked and administered by:
text
C2348343 (UMLS CUI [1])
Dose checked and witnessed by
Item
Dose checked and witnessed by:
text
C0682356 (UMLS CUI [1,1])
C1283174 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
Comments
Item
Comments:
text
C0947611 (UMLS CUI [1])

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