ID

30893

Descrizione

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. 02/07/18 02/07/18 -
Titolare del copyright

GlaxoSmithKline

Caricato su

2 luglio 2018

DOI

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Licenza

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
Descrizione

DATE OF VISIT/ASSESSMENT

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

Date of visit

Tipo di dati

date

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

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?
Descrizione

concomitant medication

Tipo di dati

text

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

adverse events

Tipo di dati

text

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

hematology; clinical chemistry

Tipo di dati

text

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

urinalysis

Tipo di dati

text

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

ECG

Tipo di dati

text

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

vital signs

Tipo di dati

text

Alias
UMLS CUI [1]
C0518766

Similar models

Logs and Repeats (Logs/Rpts)

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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