ID

30582

Beskrivning

Study part: Local Laboratory- Hematology (Lab H). 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.

Nyckelord

  1. 2018-06-16 2018-06-16 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

16 juni 2018

DOI

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Licens

Creative Commons BY-NC 3.0

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Local Laboratory- Hematology (Lab H) Pazopanib Macular Degeneration MD1103367

Local Laboratory- Hematology (Lab H)

HAEMATOLOGY
Beskrivning

HAEMATOLOGY

Alias
UMLS CUI-1
C0018941
Study part
Beskrivning

Study part

Datatyp

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C0449719
Laboratory ID
Beskrivning

Laboratory ID

Datatyp

text

Alias
UMLS CUI [1]
C2986056
Laboratory name and address
Beskrivning

Laboratory name address

Datatyp

integer

Alias
UMLS CUI [1,1]
C3258037
UMLS CUI [1,2]
C1442065
Laboratory name and address
Beskrivning

Laboratory name address

Datatyp

text

Alias
UMLS CUI [1,1]
C3258037
UMLS CUI [1,2]
C1442065
Date and time sample taken
Beskrivning

Date and time sample taken

Datatyp

datetime

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0040223
UMLS CUI [1,3]
C0200345
Has the subject fasted?
Beskrivning

Fasting

Datatyp

text

Alias
UMLS CUI [1]
C0015663
Analysis
Beskrivning

Analysis

Datatyp

text

Alias
UMLS CUI [1]
C0936012
Result Type
Beskrivning

Result Type

Datatyp

integer

Alias
UMLS CUI [1,1]
C1274040
UMLS CUI [1,2]
C0332307
If Numeric result, value:
Beskrivning

Numeric result

Datatyp

integer

Alias
UMLS CUI [1]
C2347373
If Character result, value:
Beskrivning

Character result

Datatyp

text

Alias
UMLS CUI [1]
C2350015

Similar models

Local Laboratory- Hematology (Lab H)

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
HAEMATOLOGY
C0018941 (UMLS CUI-1)
Item
Study part
text
C0008976 (UMLS CUI [1,1])
C0449719 (UMLS CUI [1,2])
Code List
Study part
CL Item
Pre-treatment (Pre-treatment)
CL Item
Days 4 (Days 4)
CL Item
Days 7 (Days 7)
CL Item
Days 10 (Pre-dose) (Days 10 (Pre-dose))
CL Item
Days 14 (+24h) (Days 14 (+24h))
CL Item
Follow-up (Follow-up)
Laboratory ID
Item
Laboratory ID
text
C2986056 (UMLS CUI [1])
Item
Laboratory name and address
integer
C3258037 (UMLS CUI [1,1])
C1442065 (UMLS CUI [1,2])
Code List
Laboratory name and address
CL Item
Results from the same lab as in the previous visit  (98)
CL Item
Please provide name and address, when not (99)
Laboratory name address
Item
Laboratory name and address
text
C3258037 (UMLS CUI [1,1])
C1442065 (UMLS CUI [1,2])
Date and time sample taken
Item
Date and time sample taken
datetime
C0011008 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,3])
Item
Has the subject fasted?
text
C0015663 (UMLS CUI [1])
Code List
Has the subject fasted?
CL Item
Yes (Y)
CL Item
No (N)
Item
Analysis
text
C0936012 (UMLS CUI [1])
Code List
Analysis
CL Item
WBC (WBC)
C0023508 (UMLS CUI-1)
(Comment:en)
CL Item
RBC (RBC)
C0014772 (UMLS CUI-1)
(Comment:en)
CL Item
Haemoglobin (Haemoglobin)
C0518015 (UMLS CUI-1)
(Comment:en)
CL Item
Haematocrit (Haematocrit)
C0018935 (UMLS CUI-1)
(Comment:en)
CL Item
Reticulocytes (Reticulocytes)
C0206161 (UMLS CUI-1)
(Comment:en)
CL Item
Platelets (Platelets)
C0032181 (UMLS CUI-1)
(Comment:en)
CL Item
Neutrophils (Neutrophils)
C0948762 (UMLS CUI-1)
(Comment:en)
CL Item
Lymphocytes (Lymphocytes)
C0200635 (UMLS CUI-1)
(Comment:en)
CL Item
Monocytes (Monocytes)
C0200637 (UMLS CUI-1)
(Comment:en)
CL Item
Eosinophil (Eosinophil)
C0200638 (UMLS CUI-1)
(Comment:en)
CL Item
Basophils (Basophils)
C0200641 (UMLS CUI-1)
(Comment:en)
Item
Result Type
integer
C1274040 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Result Type
CL Item
Numeric result (97)
C2347373 (UMLS CUI-1)
(Comment:en)
CL Item
Character result (98)
C2350015 (UMLS CUI-1)
(Comment:en)
CL Item
No result (99)
C1274040 (UMLS CUI-1)
C1298908 (UMLS CUI-2)
(Comment:en)
Numeric result
Item
If Numeric result, value:
integer
C2347373 (UMLS CUI [1])
Character result
Item
If Character result, value:
text
C2350015 (UMLS CUI [1])

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