ID

16968

Beschrijving

ODM derived from: http://research.uic.edu/qip/toolbox/case-report-forms-crf. Template Name: Adverse Events. QIP Case Report Forms, UIC Quality Improvement CRF, Office of the Vice Chancellor for Research. Center for Clinical and Translational Science, UIC University of Illinois at Chicago.

Link

http://research.uic.edu/qip/toolbox/case-report-forms-crf

Trefwoorden

  1. 17-08-16 17-08-16 -
Geüploaded op

17 augustus 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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Adverse Events: UIC Quality Improvement CRF

Adverse Events: UIC Quality Improvement CRF

General Information
Beschrijving

General Information

Protocol Title
Beschrijving

Protocol Title

Datatype

text

Site Number
Beschrijving

Site Number

Datatype

integer

Subject ID
Beschrijving

Subject ID

Datatype

integer

Visit Date
Beschrijving

Visit Date

Datatype

date

Has the subject had any Adverse Events during this study? (See description)
Beschrijving

(If yes, please list all Adverse Events below)

Datatype

boolean

Adverse Events
Beschrijving

Adverse Events

Event Description
Beschrijving

Event Description

Datatype

text

Start Date
Beschrijving

Start Date

Datatype

date

Severity (see Description)
Beschrijving

1= Mild 2= Moderate 3= Severe

Datatype

integer

Action Taken: None
Beschrijving

Action Taken

Datatype

boolean

Action Taken
Beschrijving

Action Taken: Discontinued permanently

Datatype

boolean

Action Taken: Interrupted temporarily
Beschrijving

Action Taken

Datatype

boolean

Action Taken: Reduced Dose
Beschrijving

Action Taken

Datatype

boolean

Action Taken: Increased Dose
Beschrijving

Action Taken

Datatype

boolean

Action Taken: Delayed Dose
Beschrijving

Action Taken

Datatype

boolean

Final Outcome (see Description)
Beschrijving

1= Resolved, No Sequelae 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

Datatype

integer

Stop Date
Beschrijving

Stop Date

Datatype

date

OR: Continuing
Beschrijving

OR: Continuing

Datatype

boolean

Event Analysis: Relationship to Study Intervention (see Description)
Beschrijving

Event Analysis: Relationship to Study Intervention (see Description)

Datatype

text

Event Analysis: Expected?
Beschrijving

Event Analysis: Expected?

Datatype

text

Event Analysis: Serious Adverse Event?
Beschrijving

Event Analysis: Serious Adverse Event?

Datatype

text

PI Initials
Beschrijving

PI Initials

Datatype

text

Similar models

Adverse Events: UIC Quality Improvement CRF

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
General Information
Protocol Title
Item
Protocol Title
text
Site Number
Item
Site Number
integer
Subject ID
Item
Subject ID
integer
Visit Date
Item
Visit Date
date
Has the subject had any Adverse Events during this study? (See description)
Item
Has the subject had any Adverse Events during this study? (See description)
boolean
Item Group
Adverse Events
Event Description
Item
Event Description
text
Start Date
Item
Start Date
date
Severity (see Description)
Item
Severity (see Description)
integer
Action Taken
Item
Action Taken: None
boolean
Action Taken
Item
boolean
Action Taken
Item
Action Taken: Interrupted temporarily
boolean
Action Taken
Item
Action Taken: Reduced Dose
boolean
Action Taken
Item
Action Taken: Increased Dose
boolean
Action Taken
Item
Action Taken: Delayed Dose
boolean
Final Outcome (see Description)
Item
Final Outcome (see Description)
integer
Stop Date
Item
Stop Date
date
OR: Continuing
Item
OR: Continuing
boolean
Item
Event Analysis: Relationship to Study Intervention (see Description)
text
Code List
Event Analysis: Relationship to Study Intervention (see Description)
CL Item
Definitely related (1)
CL Item
Possibly related (2)
CL Item
Not related (3)
Item
Event Analysis: Expected?
text
Code List
Event Analysis: Expected?
CL Item
Yes (1)
CL Item
No (2)
Item
Event Analysis: Serious Adverse Event?
text
Code List
Event Analysis: Serious Adverse Event?
CL Item
Yes (Complete an SAE report form) (1)
CL Item
No (2)
PI Initials
Item
PI Initials
text

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