Investigational Product and Treatment Confirmation

Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Date of Visit/Assessment
Descripción

Date of Visit/Assessment

Tipo de datos

date

Alias
UMLS CUI [1]
C1320303
UMLS CUI [2]
C2985720
Site
Descripción

Study site

Tipo de datos

text

Alias
UMLS CUI [1]
C2825164
Patient
Descripción

Patient

Tipo de datos

text

Alias
UMLS CUI [1]
C1299487
Patient No.
Descripción

Subject No.

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Study Visit
Descripción

Type of Visit

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0332307
Investigational Product
Descripción

Investigational Product

Alias
UMLS CUI-1
C0304229
Date/time of dose
Descripción

Date/time of investigational product dose

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1264639
Treatment Confirmation
Descripción

Treatment Confirmation

Alias
UMLS CUI-1
C0750484
UMLS CUI-2
C0087111
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Descripción

If no, record reasons below

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2349182
Record reason(s)
Descripción

if applicable

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C3827420

Similar models

Investigational Product and Treatment Confirmation

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Date of Visit/Assessment
Item
Date of Visit/Assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
Study site
Item
Site
text
C2825164 (UMLS CUI [1])
Patient
Item
Patient
text
C1299487 (UMLS CUI [1])
Subject No.
Item
Patient No.
text
C2348585 (UMLS CUI [1])
Item
Study Visit
text
C0545082 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Study Visit
CL Item
Visit 2 (Visit 2)
CL Item
Visit 3 (Visit 3)
CL Item
Visit 8 (Visit 8)
Item Group
Investigational Product
C0304229 (UMLS CUI-1)
Date/time of investigational product dose
Item
Date/time of dose
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Item Group
Treatment Confirmation
C0750484 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
Correct treatment?
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
boolean
C0087111 (UMLS CUI [1,1])
C2349182 (UMLS CUI [1,2])
Reason incorrect treatment
Item
Record reason(s)
text
C0566251 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C3827420 (UMLS CUI [1,3])