ID

30893

Beschrijving

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.

Trefwoorden

  1. 02-07-18 02-07-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

2 juli 2018

DOI

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Licentie

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
Beschrijving

DATE OF VISIT/ASSESSMENT

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

Date of visit

Datatype

date

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

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?
Beschrijving

concomitant medication

Datatype

text

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

adverse events

Datatype

text

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

hematology; clinical chemistry

Datatype

text

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

urinalysis

Datatype

text

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

ECG

Datatype

text

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

vital signs

Datatype

text

Alias
UMLS CUI [1]
C0518766

Similar models

Logs and Repeats (Logs/Rpts)

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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