English

Period 2 Days 16-21

1 forms  
  1. StudyEvent: ODM
    1. Period 2 Days 16-21
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Description

Clinical Trial Subject Unique Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
Investigational Product
Description

Investigational Product

Alias
UMLS CUI-1
C0304229
Planned Relative Time
Description

Experimental drug, Relative time, Planned

Data type

text

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

Experimental drug, Dosage, Date in time

Data type

date

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

Experimental drug, Dosage, Time

Data type

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0040223
Back to the top of the page

Similar models

Period 2 Days 16-21

1 forms
  1. StudyEvent: ODM
    1. Period 2 Days 16-21
Name
Type
Description | Question | Decode (Coded Value)
Data type
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 16 - AM (1)
CL Item
Day 16 - PM  (2)
CL Item
Day 17 - AM (3)
CL Item
Day 17 - PM (4)
CL Item
Day 18 - AM (5)
CL Item
Day 18 - PM (6)
CL Item
Day 19 - AM (7)
CL Item
Day 19 - PM (8)
CL Item
Day 20 - AM (9)
CL Item
Day 20 - PM (10)
CL Item
Day 21 - AM (11)
CL Item
Day 21 - PM (12)
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])
Back to the top of the page