ID

43889

Beskrivning

Study Part: Prior Parkinson’s Medication Screening. 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. 2017-10-16 2017-10-16 -
  2. 2021-09-20 2021-09-20 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

20 september 2021

DOI

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Licens

Creative Commons BY-NC 3.0

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Prior Parkinson’s Medication Screening Ropinirole Parkinson Disease 101468/165

Prior Parkinson’s Medication Screening

PRIOR PARKINSON’S MEDICATION
Beskrivning

PRIOR PARKINSON’S MEDICATION

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0030567
Patient Number
Beskrivning

Patient Number

Datatyp

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Beskrivning

Centre Number

Datatyp

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Has the subject taken any Parkinson’s medication within 30 days PRIOR to the study?
Beskrivning

Medication Parkinson Disease

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0030567
Drug Name
Beskrivning

Drug Name

Datatyp

text

Alias
UMLS CUI [1]
C2360065
SINGLE Dose/Unit
Beskrivning

dose

Datatyp

text

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

dose frequency

Datatyp

text

Alias
UMLS CUI [1]
C2826654
Route
Beskrivning

IA = intra-articular IAR = intra-arterial ID = intra-dermal IH = inhalation IM = intra-muscular IT = intra-thecal IV = intra-venous NA = nasal PO = oral PR = rectal SC = subcutaneous SL = sublingual TD = transdermal TO = topical VA = vaginal

Datatyp

text

Alias
UMLS CUI [1]
C0013153
Indication- Parkinson’s
Beskrivning

Indication

Datatyp

boolean

Alias
UMLS CUI [1]
C3146298
Duration of Therapy
Beskrivning

Duration of Therapy

Datatyp

text

Alias
UMLS CUI [1]
C0444921
End Date
Beskrivning

End Date

Datatyp

date

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

Continuing at end of study

Datatyp

boolean

Alias
UMLS CUI [1]
C1553904

Similar models

Prior Parkinson’s Medication Screening

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
PRIOR PARKINSON’S MEDICATION
C0013227 (UMLS CUI-1)
C0030567 (UMLS CUI-2)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Medication Parkinson Disease
Item
Has the subject taken any Parkinson’s medication within 30 days PRIOR to the study?
boolean
C0013227 (UMLS CUI [1,1])
C0030567 (UMLS CUI [1,2])
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
dose
Item
SINGLE Dose/Unit
text
C3174092 (UMLS CUI [1])
dose frequency
Item
Frequency of this Dose
text
C2826654 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Indication
Item
Indication- Parkinson’s
boolean
C3146298 (UMLS CUI [1])
Duration of Therapy
Item
Duration of Therapy
text
C0444921 (UMLS CUI [1])
End Date
Item
End Date
date
C0806020 (UMLS CUI [1])
Continuing at end of study
Item
Continuing at end of study?
boolean
C1553904 (UMLS CUI [1])

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