ID

30893

Beschreibung

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.

Stichworte

  1. 02.07.18 02.07.18 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

2. Juli 2018

DOI

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Lizenz

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
Beschreibung

DATE OF VISIT/ASSESSMENT

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

Date of visit

Datentyp

date

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

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?
Beschreibung

concomitant medication

Datentyp

text

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

adverse events

Datentyp

text

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

hematology; clinical chemistry

Datentyp

text

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

urinalysis

Datentyp

text

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

ECG

Datentyp

text

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

vital signs

Datentyp

text

Alias
UMLS CUI [1]
C0518766

Ähnliche Modelle

Logs and Repeats (Logs/Rpts)

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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