ID

25559

Beskrivning

Study part: Concomitant Medication. A Single Blind, Parallel Group, Up-titration, Phase 1 Study in Healthy Volunteers to Determine a Starting Dose and Select an Up-titration Regimen for a new Formulation of Ropinirole. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Phase: phase 1. Study Recruitment Status: Completed Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP, Zygara; Zygara, ZIPEREVE, ZEPREVE, Requip Depot, REQUIP, REPREVE, Modutab, ADARTREL. Study Indication : Restless Legs Syndrome. Study ID: 101468/201. Clinical Study ID: 101468/201

Nyckelord

Versioner (2)
  1. 2017-09-05 2017-09-05 -
  2. 2019-05-10 2019-05-10 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

5 september 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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Concomitant Medication Ropinirole Restless Legs Syndrome 101468/201

Engelsk

Concomitant Medication

1 Formulär  
  1. StudyEvent: ODM
    1. Concomitant Medication
CONCOMITANT MEDICATION
Beskrivning

CONCOMITANT MEDICATION

Alias
UMLS CUI-1
C2347852
Subject number
Beskrivning

Subject number

Datatyp

integer

Alias
UMLS CUI [1]
C2348585
Are there any concomitant medication changes since the start of the study?
Beskrivning

Concomitant Medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2347852
Drug Name
Beskrivning

Drug Name

Datatyp

text

Alias
UMLS CUI [1]
C0013227
Single dose/Unit
Beskrivning

Single dose

Datatyp

text

Alias
UMLS CUI [1]
C1960417
Frequency of this dose
Beskrivning

dose frequency

Datatyp

text

Alias
UMLS CUI [1]
C2826654
Route
Beskrivning

Route

Datatyp

text

Alias
UMLS CUI [1]
C0013153
Indication
Beskrivning

Indication

Datatyp

text

Alias
UMLS CUI [1]
C3146298
Start Date/Time
Beskrivning

Start Date and Time

Datatyp

datetime

Alias
UMLS CUI [1]
C3897500
End Date/Time
Beskrivning

End Date and Time

Datatyp

datetime

Alias
UMLS CUI [1]
C3899266
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Similar models

Concomitant Medication

1 Formulär
  1. StudyEvent: ODM
    1. Concomitant Medication
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
CONCOMITANT MEDICATION
C2347852 (UMLS CUI-1)
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
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
C0013227 (UMLS CUI [1])
Single dose
Item
Single dose/Unit
text
C1960417 (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
text
C3146298 (UMLS CUI [1])
Start Date and Time
Item
Start Date/Time
datetime
C3897500 (UMLS CUI [1])
End Date and Time
Item
End Date/Time
datetime
C3899266 (UMLS CUI [1])
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