Englisch

Period 2 Days 65-67

1 Formulare  
  1. StudyEvent: ODM
    1. Period 2 Days 65-67
Administrative Data
Beschreibung

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Beschreibung

Clinical Trial Subject Unique Identifier

Datentyp

integer

Alias
UMLS CUI [1]
C2348585
Investigational Product
Beschreibung

Investigational Product

Alias
UMLS CUI-1
C0304229
Planned Relative Time
Beschreibung

Experimental drug, Relative time, Planned

Datentyp

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0439564
UMLS CUI [1,3]
C1301732
Date of Dose
Beschreibung

Experimental drug, Dosage, Date in time

Datentyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
Time of Dose
Beschreibung

Experimental drug, Dosage, Time

Datentyp

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0040223
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Ähnliche Modelle

Period 2 Days 65-67

1 Formulare
  1. StudyEvent: ODM
    1. Period 2 Days 65-67
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
Investigational Product
C0304229 (UMLS CUI-1)
Item
Planned Relative Time
text
C0304229 (UMLS CUI [1,1])
C0439564 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
Experimental drug, Relative time, Planned
Code List
Planned Relative Time
CL Item
Day 65 - AM (1)
CL Item
Day 65 - PM  (2)
CL Item
Day 66 - AM (3)
CL Item
Day 66 - PM (4)
CL Item
Day 67 - AM (5)
CL Item
Day 67 - PM (6)
Experimental drug, Dosage, Date in time
Item
Date of Dose
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Experimental drug, Dosage, Time
Item
Time of Dose
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
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