ID

40864

Description

Study ID: 101468/902 Clinical Study ID: 101468/902 Study Title:A study to evaluate the effect of repeated oral doses of ropinirole on cardiac conduction as assessed by 12-lead electrocardiogram compared to placebo and single oral doses of moxifloxacin (Bayer) as a positive control. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline 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

Keywords

  1. 5/27/20 5/27/20 -
Copyright Holder

GlaxoSmithKline

Uploaded on

May 27, 2020

DOI

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License

Creative Commons BY-NC 4.0

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Effect of ropinirole on cardiac conduction as assessed by 12-lead electrocardiogram (101468/902)

Dosing Details

  1. StudyEvent: ODM
    1. Dosing Details
Administrative
Description

Administrative

Alias
UMLS CUI-1
C1320722
Subject Number
Description

Subject Number

Data type

text

Alias
UMLS CUI [1]
C2348585
Dosing Details
Description

Dosing Details

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0178602
Dosing - Day
Description

Dosing - Day

Data type

integer

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0439228
Dosing - Date
Description

Dosing - Date

Data type

date

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0011008
Time of dosing
Description

Time of dosing

Data type

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Dosing - Comments
Description

Dosing - Comments

Data type

text

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0947611

Similar models

Dosing Details

  1. StudyEvent: ODM
    1. Dosing Details
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Item Group
Dosing Details
C0013227 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Item
Dosing - Day
integer
C0178602 (UMLS CUI [1,1])
C0439228 (UMLS CUI [1,2])
Code List
Dosing - Day
CL Item
Day 2 (1)
CL Item
Day 4 (2)
CL Item
Day 5 (3)
CL Item
Day 6 (4)
CL Item
Day7 (5)
Dosing - Date
Item
Dosing - Date
date
C0178602 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of dosing
Item
Time of dosing
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosing - Comments
Item
Dosing - Comments
text
C0178602 (UMLS CUI [1,1])
C0947611 (UMLS CUI [1,2])

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