ID

26206

Descripción

A sample trial to demonstrate the end-to-end application of the CDISC Standards and transformations from ADL

Palabras clave

  1. 11/10/17 11/10/17 - Philipp Bruland
Titular de derechos de autor

Unknown

Subido en

11 de octubre de 2017

DOI

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Licencia

Creative Commons BY-NC-ND 3.0

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Sample Study

Adverse Events

Common
Descripción

Common

Alias
TEST
Common ItemGroup Alias
Site number
Descripción

Site Number as assigned by CRO

Tipo de datos

integer

Alias
SDTM
SITEID
Subject ID
Descripción

Subject ID

Tipo de datos

text

Alias
SDTM
USUBJID
Visit Date
Descripción

Visit Date

Tipo de datos

date

Visit Start Time
Descripción

Visit Time

Tipo de datos

time

Adverse events
Descripción

Adverse events

Has the subject experienced any adverse events
Descripción

Adverse Event Experienced

Tipo de datos

integer

Adverse events
Descripción

Adverse events

Event No.
Descripción

Adverse Event Number

Tipo de datos

integer

Adverse event
Descripción

Adverse Event Term

Tipo de datos

text

Start Date
Descripción

Adverse Event Start Date

Tipo de datos

date

Is the adverse event still continuing
Descripción

Adverse Event Continues

Tipo de datos

integer

Stop Date
Descripción

Adverse Event Stop Date

Tipo de datos

date

Duration of the adverse event
Descripción

AE duration

Tipo de datos

durationDatetime

Was event serious
Descripción

Adverse Event Serious

Tipo de datos

integer

Severity
Descripción

Adverse Event Severity

Tipo de datos

integer

Action taken with study drug
Descripción

Adverse Event Action Taken

Tipo de datos

integer

Subject outcome
Descripción

Adverse Event Subject Outcome

Tipo de datos

integer

Similar models

Adverse Events

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Common
Common ItemGroup Alias (TEST)
Site Number
Item
Site number
integer
SITEID (SDTM)
Subject ID
Item
Subject ID
text
USUBJID (SDTM)
Visit Date
Item
Visit Date
date
Visit Time
Item
Visit Start Time
time
Item Group
Adverse events
Item
Has the subject experienced any adverse events
integer
Code List
Has the subject experienced any adverse events
CL Item
No (0)
CL Item
Yes (1)
Item Group
Adverse events
Adverse Event Number
Item
Event No.
integer
Adverse Event Term
Item
Adverse event
text
Adverse Event Start Date
Item
Start Date
date
Item
Is the adverse event still continuing
integer
Code List
Is the adverse event still continuing
CL Item
No (0)
CL Item
Yes (1)
Adverse Event Stop Date
Item
Stop Date
date
AE duration
Item
Duration of the adverse event
durationDatetime
Item
Was event serious
integer
Code List
Was event serious
CL Item
No (0)
CL Item
Yes (1)
Item
Severity
integer
Code List
Severity
CL Item
Mild (1)
CL Item
Moderate (2)
CL Item
Severe (3)
Item
Is there a reasonable possibility that the AE may have been caused by the study drug
integer
Code List
Is there a reasonable possibility that the AE may have been caused by the study drug
CL Item
No (0)
CL Item
Yes (1)
Item
Action taken with study drug
integer
Code List
Action taken with study drug
CL Item
None (1)
CL Item
Study drug regimen changed (2)
CL Item
Temporarily stopped study drug (3)
CL Item
Study drug discontinued (4)
Item
Subject outcome
integer
Code List
Subject outcome
CL Item
Subject remains in study (1)
CL Item
Withdrawn from study (2)
CL Item
Lost to follow-up (3)
CL Item
Death (4)

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