ID

25360

Description

Study part: AE/ Concomitant Medication Probe Week 1 Day 1. 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

Keywords

Versions (2)
  1. 9/2/17 9/2/17 -
  2. 6/19/19 6/19/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 2, 2017

DOI

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License

Creative Commons BY-NC 3.0
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AE/ Concomitant Medication Probe Week 1 Day 1 Ropinirole Restless Legs Syndrome 101468/201

English

AE/ Concomitant Medication Probe Week 1 Day 1

1 forms  
AE / CONCOMITANT MEDICATION PROBE
Description

AE / CONCOMITANT MEDICATION PROBE

Alias
UMLS CUI-1
C2347852
Subject number
Description

Subject number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Time relative to start of dose- Pre-dose- Subject asked?
Description

time dosage

Data type

boolean

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0178602
If no, comment
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Time relative to start of dose- +2 hrs - Subject asked?
Description

time dosage

Data type

boolean

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0178602
If no, comment
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Time relative to start of dose- +6 hrs - Subject asked?
Description

time dosage

Data type

boolean

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0178602
If no, comment
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Time relative to start of dose- +16 hrs - Subject asked?
Description

time dosage

Data type

boolean

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0178602
If no, comment
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
Time relative to start of dose- +24 hrs (prior to next dose)- Subject asked?
Description

time dosage

Data type

boolean

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0178602
If no, comment
Description

comment

Data type

text

Alias
UMLS CUI [1]
C0947611
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Similar models

AE/ Concomitant Medication Probe Week 1 Day 1

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
AE / CONCOMITANT MEDICATION PROBE
C2347852 (UMLS CUI-1)
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
time dosage
Item
Time relative to start of dose- Pre-dose- Subject asked?
boolean
C0040223 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
comment
Item
If no, comment
text
C0947611 (UMLS CUI [1])
time dosage
Item
Time relative to start of dose- +2 hrs - Subject asked?
boolean
C0040223 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
comment
Item
If no, comment
text
C0947611 (UMLS CUI [1])
time dosage
Item
Time relative to start of dose- +6 hrs - Subject asked?
boolean
C0040223 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
comment
Item
If no, comment
text
C0947611 (UMLS CUI [1])
time dosage
Item
Time relative to start of dose- +16 hrs - Subject asked?
boolean
C0040223 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
comment
Item
If no, comment
text
C0947611 (UMLS CUI [1])
time dosage
Item
Time relative to start of dose- +24 hrs (prior to next dose)- Subject asked?
boolean
C0040223 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
comment
Item
If no, comment
text
C0947611 (UMLS CUI [1])
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