ID

30893

Description

Study part: Logs and Repeats (Logs/Rpts). A phase 1 single-masked, randomized (with respect to placebo), placebo-controlled, parallel-group, dose-rising study to evaluate the safety, tolerability and pharmacokinetics of repeat oral doses of GW786034 in elderly healthy volunteers. Trade Name: Votrient. Clinical Study ID: MD1103367.

Keywords

  1. 7/2/18 7/2/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 2, 2018

DOI

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License

Creative Commons BY-NC 3.0

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Logs and Repeats (Logs/Rpts) Pazopanib Macular Degeneration MD1103367

Logs and Repeats (Logs/Rpts)

DATE OF VISIT/ASSESSMENT
Description

DATE OF VISIT/ASSESSMENT

Alias
UMLS CUI-1
C1320303
Date of visit/assessment
Description

Date of visit

Data type

date

Alias
UMLS CUI [1]
C1320303
ADVERSE EVENT/CONCOMITANT MEDICATION/REPEAT ASSESSMENT CHECK QUESTIONS
Description

ADVERSE EVENT/CONCOMITANT MEDICATION/REPEAT ASSESSMENT CHECK QUESTIONS

Alias
UMLS CUI-1
C0877248
UMLS CUI-3
C2347852
UMLS CUI-5
C0681799
Were any concomitant medications taken by the subject during the study?
Description

concomitant medication

Data type

text

Alias
UMLS CUI [1]
C2347852
Did the subject experience any adverse events during the study?
Description

adverse events

Data type

text

Alias
UMLS CUI [1]
C0877248
Were any repeat haematology or clinical chemistry samples taken?
Description

hematology; clinical chemistry

Data type

text

Alias
UMLS CUI [1]
C0474523
UMLS CUI [2]
C0008000
Were any repeat urinalysis sample taken?
Description

urinalysis

Data type

text

Alias
UMLS CUI [1]
C0042014
Were any repeat ECGs performed?
Description

ECG

Data type

text

Alias
UMLS CUI [1]
C1623258
Were any repeat vital signs recorded?
Description

vital signs

Data type

text

Alias
UMLS CUI [1]
C0518766

Similar models

Logs and Repeats (Logs/Rpts)

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
DATE OF VISIT/ASSESSMENT
C1320303 (UMLS CUI-1)
Date of visit
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1])
Item Group
ADVERSE EVENT/CONCOMITANT MEDICATION/REPEAT ASSESSMENT CHECK QUESTIONS
C0877248 (UMLS CUI-1)
C2347852 (UMLS CUI-3)
C0681799 (UMLS CUI-5)
Item
Were any concomitant medications taken by the subject during the study?
text
C2347852 (UMLS CUI [1])
Code List
Were any concomitant medications taken by the subject during the study?
CL Item
Yes (Y)
CL Item
No (N)
Item
Did the subject experience any adverse events during the study?
text
C0877248 (UMLS CUI [1])
Code List
Did the subject experience any adverse events during the study?
CL Item
Yes (Y)
CL Item
No (N)
Item
Were any repeat haematology or clinical chemistry samples taken?
text
C0474523 (UMLS CUI [1])
C0008000 (UMLS CUI [2])
Code List
Were any repeat haematology or clinical chemistry samples taken?
CL Item
Yes (Y)
CL Item
No (N)
Item
Were any repeat urinalysis sample taken?
text
C0042014 (UMLS CUI [1])
Code List
Were any repeat urinalysis sample taken?
CL Item
Yes (Y)
CL Item
No (N)
Item
Were any repeat ECGs performed?
text
C1623258 (UMLS CUI [1])
Code List
Were any repeat ECGs performed?
CL Item
Yes (Y)
CL Item
No (N)
Item
Were any repeat vital signs recorded?
text
C0518766 (UMLS CUI [1])
Code List
Were any repeat vital signs recorded?
CL Item
Yes (Y)
CL Item
No (N)

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