ID

9230

Descrição

Adverse Events (AE) Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=B1267264-7F67-522F-E034-0003BA12F5E7

Link

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=B1267264-7F67-522F-E034-0003BA12F5E7

Palavras-chave

Versões (2)
  1. 19/09/2012 19/09/2012 -
  2. 09/01/2015 09/01/2015 - Martin Dugas
Transferido a

9 de janeiro de 2015

DOI

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Licença

Creative Commons BY-NC 3.0 Legacy
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Melanoma (Skin) null Toxicity - Adverse Events (AE) - 2074863v3.0

Inglês

No Instruction available.

1 Formulários  
  1. StudyEvent: Adverse Events (AE)
    1. No Instruction available.
Ccrr Module For Adverse Events (ae)
Descrição

Ccrr Module For Adverse Events (ae)

Patient ID (Pt. ID issued during registration or previously issued patient ID)
Descrição

Pt.ID

Tipo de dados

text

Institution ID
Descrição

InstitutionNo.

Tipo de dados

text

Alias
NCI Thesaurus ValueDomain
C25337
UMLS 2011AA ValueDomain
C0237753
Patient Initials (F ML)
Descrição

Patient Initials

Tipo de dados

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Institution:
Descrição

InstitutionName

Tipo de dados

text

Date of patient evaluation (Month Year Day)
Descrição

AssessmentDate

Tipo de dados

date

Has the patient experienced any adverse events since the last visit (Adverse Event Text)
Descrição

LateAdverseEventInd

Tipo de dados

boolean

Grade
Descrição

CTCAdverseEventGrade

Tipo de dados

text

Serious (If AE is serious, also report through AdEERS)
Descrição

Serious

Tipo de dados

boolean

Relationship to Study Intervention
Descrição

CTCAdverseEventAttributionCode

Tipo de dados

text

Present Status
Descrição

CTCAdverseEventOutcome

Tipo de dados

text

Alias
NCI Thesaurus ObjectClass
C41331
UMLS 2011AA ObjectClass
C0877248
NCI Thesaurus Property
C20200
UMLS 2011AA Property
C1274040
Other (specify in Comments)
Descrição

OtherInd-3

Tipo de dados

text

Alias
NCI Thesaurus ValueDomain
C25704
UMLS 2011AA ValueDomain
C1527021
NCI Thesaurus ValueDomain-2
C25180
UMLS 2011AA ValueDomain-2
C1522602
Action Taken:
Descrição

CTCAdverseEvent,ActionTaken

Tipo de dados

text

Alias
NCI Thesaurus ObjectClass
C41331
UMLS 2011AA ObjectClass
C0877248
NCI Thesaurus Property
C25404
UMLS 2011AA Property
C0441472
Other (specify in Comments)
Descrição

Other

Tipo de dados

text

MedDRA Code
Descrição

MedDRACode

Tipo de dados

text

Alias
NCI Thesaurus ValueDomain
C25162
UMLS 2011AA ValueDomain
C0805701
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
NCI Metathesaurus ObjectClass
CL104089
Onset (DATE):
Descrição

AdverseEventOnsetDate

Tipo de dados

text

Resolution (DATE):
Descrição

AdverseEventSymptomEndDate

Tipo de dados

date

Alias
NCI Thesaurus ValueDomain
C25164
UMLS 2011AA ValueDomain
C0011008
NCI Thesaurus ObjectClass
C41331
UMLS 2011AA ObjectClass
C0877248
NCI Thesaurus Property
C4876
UMLS 2011AA Property
C1457887
Onset Date reported at a prior visit
Descrição

OnsetDatereportedatapriorvisit

Tipo de dados

text

still present at this visit (Month Year Day)
Descrição

stillpresentatthisvisit

Tipo de dados

text

Comments:
Descrição

Comments

Tipo de dados

text

Completed by:
Descrição

CompletedBy

Tipo de dados

text

Date:
Descrição

FormCompletionDate,Original

Tipo de dados

date

Month Year Day
Descrição

MonthYearDay

Tipo de dados

text

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Similar models

No Instruction available.

1 Formulários
  1. StudyEvent: Adverse Events (AE)
    1. No Instruction available.
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Ccrr Module For Adverse Events (ae)
Pt.ID
Item
Patient ID (Pt. ID issued during registration or previously issued patient ID)
text
InstitutionNo.
Item
Institution ID
text
C25337 (NCI Thesaurus ValueDomain)
C0237753 (UMLS 2011AA ValueDomain)
Patient Initials
Item
Patient Initials (F ML)
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
InstitutionName
Item
Institution:
text
AssessmentDate
Item
Date of patient evaluation (Month Year Day)
date
LateAdverseEventInd
Item
Has the patient experienced any adverse events since the last visit (Adverse Event Text)
boolean
Item
Grade
text
CL.2
Code List
Grade
CL Item
Mild (Mild)
CL Item
Moderate (Moderate)
CL Item
Severe (Severe)
CL Item
Life-threatening or disabling (Life-threatening or disabling)
CL Item
Fatal (Fatal)
Serious
Item
Serious (If AE is serious, also report through AdEERS)
boolean
Item
Relationship to Study Intervention
text
CL.4
Code List
Relationship to Study Intervention
CL Item
Unrelated (Unrelated)
C25328 (NCI Thesaurus)
C0445356 (UMLS 2011AA)
CL Item
Unlikely (Unlikely)
CL Item
Possibly (Possibly)
CL Item
Probably (Probably)
CL Item
Definitely (Definitely)
CL Item
Unknown/Not Applicable (Unknown/Not Applicable)
Item
Present Status
text
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C20200 (NCI Thesaurus Property)
C1274040 (UMLS 2011AA Property)
CL.5
Code List
Present Status
CL Item
Adverse Event Was Fatal (Fatal/Died)
CL Item
Adverse Event Is Ongoing (Intervention for AE continues)
CL Item
Adverse Event Is Unchanged (Not recovered/Not resolved)
CL Item
Adverse Event Is Resolved With Sequelae (Recovered/Resolved with sequelae)
CL Item
Adverse Event Is Resolved (Recovered/Resolved without sequelae)
CL Item
Adverse Event Has Improved (Recovering/Resolving)
CL Item
Other (specify in Comments) (Other (specify in Comments))
OtherInd-3
Item
Other (specify in Comments)
text
C25704 (NCI Thesaurus ValueDomain)
C1527021 (UMLS 2011AA ValueDomain)
C25180 (NCI Thesaurus ValueDomain-2)
C1522602 (UMLS 2011AA ValueDomain-2)
Item
Action Taken:
text
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C25404 (NCI Thesaurus Property)
C0441472 (UMLS 2011AA Property)
CL.6
Code List
Action Taken:
CL Item
There Was No Action Taken Based On The Adverse Event (None)
CL Item
Protocol Treatment Was Discontinued As A Result Of The Adverse Event (Early termination)
CL Item
Concomitant medications (Concomitant medications)
CL Item
Hospitalization (Hospitalization)
CL Item
Other (specify in Comments) (Other (specify in Comments))
Other
Item
Other (specify in Comments)
text
MedDRACode
Item
MedDRA Code
text
C25162 (NCI Thesaurus ValueDomain)
C0805701 (UMLS 2011AA ValueDomain)
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
CL104089 (NCI Metathesaurus ObjectClass)
AdverseEventOnsetDate
Item
Onset (DATE):
text
AdverseEventSymptomEndDate
Item
Resolution (DATE):
date
C25164 (NCI Thesaurus ValueDomain)
C0011008 (UMLS 2011AA ValueDomain)
C41331 (NCI Thesaurus ObjectClass)
C0877248 (UMLS 2011AA ObjectClass)
C4876 (NCI Thesaurus Property)
C1457887 (UMLS 2011AA Property)
OnsetDatereportedatapriorvisit
Item
Onset Date reported at a prior visit
text
stillpresentatthisvisit
Item
still present at this visit (Month Year Day)
text
Comments
Item
Comments:
text
CompletedBy
Item
Completed by:
text
FormCompletionDate,Original
Item
Date:
date
MonthYearDay
Item
Month Year Day
text
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