ID

16975

Description

ODM derived from: http://www.qmcr.ualberta.ca/en/ToolsandTemplates/CaseReportFormCRFTemplates.aspx. Template Name: Adverse Events. University of Alberta, Quality Management in Clinical Research. Copyright: 2002-2016 University of Alberta.

Lien

http://www.qmcr.ualberta.ca/en/ToolsandTemplates/CaseReportFormCRFTemplates.aspx

Mots-clés

  1. 17/08/2016 17/08/2016 -
Téléchargé le

17 août 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Adverse Events: CRF QMCR University of Alberta

Adverse Events: CRF QMCR University of Alberta

General Information
Description

General Information

Study Name
Description

Study Name

Type de données

text

Site Number
Description

Site Number

Type de données

integer

Pt_ID
Description

Pt_ID

Type de données

integer

Has the participant had any Adverse Events during this Study? (see Description)
Description

If yes, please list all Adverse Events below.

Type de données

boolean

Adverse Events
Description

Adverse Events

Adverse Event
Description

Adverse Event

Type de données

text

Start Date
Description

Start Date

Type de données

date

Stop Date
Description

Stop Date

Type de données

date

Severity
Description

Severity

Type de données

text

Relationship to Study Treatment
Description

Relationship to Study Treatment

Type de données

text

Action Taken (see Description)
Description

1= None 2= Discontinued permanently 3= Discontinued temporarily 4= Reduced Dose 5= Increased Dose 6= Delayed Dose

Type de données

integer

Outcome of AE (see Description)
Description

1= Resolved, No Sequel 2= AE still present - no treatment 3= AE still present - being treated 4= Residual effects present - not treated 5= Residual effects present - treated 6= Death 7= Unknown

Type de données

integer

Expected?
Description

Expected?

Type de données

boolean

Serious Adverse Event
Description

Serious Adverse Event

Type de données

text

Initials
Description

Initials

Type de données

text

Similar models

Adverse Events: CRF QMCR University of Alberta

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
General Information
Study Name
Item
Study Name
text
Site Number
Item
Site Number
integer
Pt_ID
Item
Pt_ID
integer
Has the participant had any Adverse Events during this Study? (see Description)
Item
Has the participant had any Adverse Events during this Study? (see Description)
boolean
Item Group
Adverse Events
Adverse Event
Item
Adverse Event
text
Start Date
Item
Start Date
date
Stop Date
Item
Stop Date
date
Item
Severity
text
Code List
Severity
CL Item
Mild (1)
CL Item
Moderate (2)
CL Item
Severe (3)
Item
Relationship to Study Treatment
text
Code List
Relationship to Study Treatment
CL Item
Definitely related (1)
CL Item
Possibly related (2)
CL Item
Not related (3)
Action Taken (see Description)
Item
Action Taken (see Description)
integer
Outcome of AE (see Description)
Item
Outcome of AE (see Description)
integer
Expected?
Item
Expected?
boolean
Item
Serious Adverse Event
text
Code List
Serious Adverse Event
CL Item
Yes (complete SAE form) (1)
CL Item
No (2)
Initials
Item
Initials
text

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