ID

10196

Descripción

OFF TREATMENT NOTICE S0023: Combination Chemo Plus RT With or Without Gefitinib in Treating Patients With Unresectable Stage III NSCLC NCT00020709 Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=9CA62D43-4EE1-361C-E034-080020C9C0E0

Link

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=9CA62D43-4EE1-361C-E034-080020C9C0E0

Palabras clave

  1. 19/9/12 19/9/12 -
  2. 30/4/15 30/4/15 - Martin Dugas
Subido en

30 de abril de 2015

DOI

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Licencia

Creative Commons BY-NC 3.0 Legacy

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Lung cancer OFF TREATMENT NCT00020709

No Instruction available.

  1. StudyEvent: OFF TREATMENT NOTICE
    1. No Instruction available.
Header
Descripción

Header

Alias
UMLS CUI-1
C1320722
SWOG Patient ID
Descripción

SWOGPatientID

Tipo de datos

text

SWOG Study No.
Descripción

SWOGStudyNo.

Tipo de datos

text

Registration Step
Descripción

Registration Step

Tipo de datos

text

Alias
NCI Thesaurus ValueDomain
C25337
NCI Thesaurus ValueDomain-2
C16154
UMLS CUI-1
C1514821
Patient Initials (L, F,M)
Descripción

PatientInitials

Tipo de datos

text

Institution / Affiliate
Descripción

Institution/Affiliate

Tipo de datos

text

Physician
Descripción

Physician

Tipo de datos

text

Group Name (Groups other than SWOG )
Descripción

GroupName

Tipo de datos

text

Study No. (Groups other than SWOG )
Descripción

Study No. (Groups other than SWOG )

Tipo de datos

text

Pt. ID (Groups other than SWOG )
Descripción

Pt.ID

Tipo de datos

text

Patient data
Descripción

Patient data

Alias
UMLS CUI-1
C2707520
Treatment Start Date
Descripción

Treatment Start Date

Tipo de datos

date

Alias
UMLS CUI-1
C3173309
Treatment End Date
Descripción

Treatment End Date

Tipo de datos

date

Alias
UMLS CUI-1
C1531784
Regimen or Procedure or Site(s)
Descripción

RegimenorProcedureorSite(s)

Tipo de datos

text

Date of Last Contact (or death)
Descripción

DateofLastContact(ordeath):

Tipo de datos

date

Alias
UMLS CUI-1
C0805839
Vital Status
Descripción

Vital Status

Tipo de datos

text

Alias
UMLS CUI-1
C1148433
Notes
Descripción

Notes

Tipo de datos

text

Off treatment
Descripción

Off treatment

Alias
UMLS CUI-1
C1518544
Off Treatment Reason (select one:)
Descripción

OffTreatmentReason

Tipo de datos

text

Alias
UMLS CUI-1
C1518544
UMLS CUI-2
C0566251
Medically required, due to toxicity, specify
Descripción

Medicallyrequired,duetotoxicity,specify:

Tipo de datos

text

Patient refused, due to toxicity, specify
Descripción

Patientrefused,duetotoxicity,specify:

Tipo de datos

text

Progression or relapse. Sites
Descripción

Progressionorrelapse.Sites:

Tipo de datos

text

Other, specify
Descripción

Other,specify:

Tipo de datos

text

Date of completion, progression, death or decision to discontinue therapy (Off Treatment Date)
Descripción

Dateofcompletion,progression,deathordecisiontodiscontinuetherapy:

Tipo de datos

date

Alias
UMLS CUI-1
C1518544
UMLS CUI-2
C0011008
Will patient receive further treatment?
Descripción

Willpatientreceivefurthertreatment?

Tipo de datos

text

Similar models

No Instruction available.

  1. StudyEvent: OFF TREATMENT NOTICE
    1. No Instruction available.
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Header
C1320722 (UMLS CUI-1)
SWOGPatientID
Item
SWOG Patient ID
text
SWOGStudyNo.
Item
SWOG Study No.
text
RegistrationStep
Item
Registration Step
text
C25337 (NCI Thesaurus ValueDomain)
C16154 (NCI Thesaurus ValueDomain-2)
C1514821 (UMLS CUI-1)
PatientInitials
Item
Patient Initials (L, F,M)
text
Institution/Affiliate
Item
Institution / Affiliate
text
Physician
Item
Physician
text
GroupName
Item
Group Name (Groups other than SWOG )
text
StudyNo.
Item
Study No. (Groups other than SWOG )
text
Pt.ID
Item
Pt. ID (Groups other than SWOG )
text
Item Group
Patient data
C2707520 (UMLS CUI-1)
TreatmentStartDate
Item
Treatment Start Date
date
C3173309 (UMLS CUI-1)
TreatmentEndDate
Item
Treatment End Date
date
C1531784 (UMLS CUI-1)
Regimen or Procedure or Site(s)
Item
Regimen or Procedure or Site(s)
text
Date of Last Contact
Item
Date of Last Contact (or death)
date
C0805839 (UMLS CUI-1)
Item
Vital Status
text
C1148433 (UMLS CUI-1)
Code List
Vital Status
CL Item
Alive (Alive)
C2584946 (UMLS CUI-1)
CL Item
Dead (Dead)
C0011065 (UMLS CUI-1)
Notes
Item
Notes
text
Item Group
Off treatment
C1518544 (UMLS CUI-1)
Item
Off Treatment Reason (select one:)
text
C1518544 (UMLS CUI-1)
C0566251 (UMLS CUI-2)
Code List
Off Treatment Reason (select one:)
CL Item
Treatment completed per protocol criteria (Treatment completed per protocol criteria)
CL Item
Medically required, due to toxicity, specify (Medically required, due to toxicity, specify)
Item
Medically required, due to toxicity, specify
text
Code List
Medically required, due to toxicity, specify
CL Item
Pt_refused_due_to_toxic2006857 (Patient refused, due to toxicity, specify)
Item
Patient refused, due to toxicity, specify
text
Code List
Patient refused, due to toxicity, specify
CL Item
Pt_refused_oth_than_tox2006859 (Patient refused, other than toxicity, specify)
CL Item
Prog_or_relapse_sites_2006860 (Progression or relapse. Sites)
Item
Progression or relapse. Sites
text
Code List
Progression or relapse. Sites
CL Item
Death_attach_notice_of_2006862 (Death (attach Notice of Death form))
CL Item
Other_specify_2006863 (Other, specify)
Other,specify:
Item
Other, specify
text
Off Treatment Date
Item
Date of completion, progression, death or decision to discontinue therapy (Off Treatment Date)
date
C1518544 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
Item
Will patient receive further treatment?
text
Code List
Will patient receive further treatment?
CL Item
No (No)
CL Item
Yes, specify (Yes, specify)
CL Item
Unknown (Unknown)

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