ID
36086
Description
Study ID: 101468/201 Clinical Study ID: 101468/201 Study Title: 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 Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A 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 The Study consists of 21 Visits(Days): Screening (Day 0) Week 1: including Day 1-7 Week 2: including Day 8-14 Week 3: including Day 15-19 Follow-up Visit (Day 21) This document contains the Laboratory Collections form. It has to be filled in for screening and Follow-up.
Keywords
Versions (2)
- 4/15/19 4/15/19 -
- 4/15/19 4/15/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
April 15, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Determination of starting dose and up-titration regimen for a new formulation of Ropinirole, 101468/201
Laboratory Collections
- StudyEvent: ODM
Description
CLINICAL CHEMISTRY and HAEMATOLOGY
Alias
- UMLS CUI-1
- C0008000
- UMLS CUI-2
- C0018941
Description
day month year
Data type
date
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0011008
Description
00:00-23:59
Data type
time
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0040223
Description
Comments
Data type
text
Alias
- UMLS CUI [1]
- C0947611
Description
If YES, please record diagnosis on Baseline Signs and Symptoms page.
Data type
text
Alias
- UMLS CUI [1]
- C0438215
Description
URINALYSIS
Alias
- UMLS CUI-1
- C0042014
Description
day month year
Data type
date
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0011008
Description
00:00-23:59
Data type
time
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0040223
Description
Comments
Data type
text
Alias
- UMLS CUI [1]
- C0947611
Description
If YES, please record diagnosis on Baseline Signs and Symptoms page.
Data type
text
Alias
- UMLS CUI [1]
- C0438142
Similar models
Laboratory Collections
- StudyEvent: ODM
C0018941 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])