ID

30270

Beskrivning

Specialized Radiation Therapy in Treating Patients With Stage II, Stage III, Stage IV, or Recurrent Non-Small Cell Lung Cancer and Poor Performance Status; ODM derived from: https://clinicaltrials.gov/show/NCT00986297

Länk

https://clinicaltrials.gov/show/NCT00986297

Nyckelord

Versioner (1)
  1. 2018-05-26 2018-05-26 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

26 maj 2018

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Lung Cancer NCT00986297

Engelsk

Eligibility Lung Cancer NCT00986297

1 Formulär  
Criteria
Beskrivning

Criteria

histologically or cytologically confirmed non-small cell lung cancer
Beskrivning

Non-Small Cell Lung Carcinoma

Datatyp

boolean

Alias
UMLS CUI [1]
C0007131
stage ii-iv and/or recurrent disease
Beskrivning

TNM clinical staging | Recurrent disease

Datatyp

boolean

Alias
UMLS CUI [1]
C3258246
UMLS CUI [2]
C0277556
no small cell histology
Beskrivning

Exclusion Cell Small Histology

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0007634
UMLS CUI [1,3]
C0700321
UMLS CUI [1,4]
C4048239
measurable or evaluable disease
Beskrivning

Measurable Disease | Evaluable Disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2]
C1516986
tumor not amenable to surgical resection
Beskrivning

Tumor Excision Unsuccessful

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C0728940
UMLS CUI [1,3]
C1272705
tumor not eligible for stereotactic body radiation therapy
Beskrivning

Tumor Ineligible Stereotactic Body Radiotherapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C1512714
UMLS CUI [1,3]
C1720823
no prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields
Beskrivning

Exclusion Criteria | Prior radiation therapy Region Neoplasm Involved | Overlap Radiation Field Current

Datatyp

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0279134
UMLS CUI [2,2]
C0205147
UMLS CUI [2,3]
C0027651
UMLS CUI [2,4]
C1314939
UMLS CUI [3,1]
C1948020
UMLS CUI [3,2]
C1882536
UMLS CUI [3,3]
C0521116
patient characteristics:
Beskrivning

Client Characteristics

Datatyp

boolean

Alias
UMLS CUI [1]
C0815172
zubrod performance status 2-4
Beskrivning

Zubrod Performance Status

Datatyp

boolean

Alias
UMLS CUI [1]
C3714786
not pregnant or nursing
Beskrivning

Pregnancy Absent | Breast Feeding Absent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0006147
UMLS CUI [2,2]
C0332197
negative pregnancy test
Beskrivning

Pregnancy test negative

Datatyp

boolean

Alias
UMLS CUI [1]
C0427780
fertile patients must agree to use effective contraception
Beskrivning

Fertility Contraceptive methods

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0700589
must complete all required pretreatment evaluations
Beskrivning

Evaluation pre treatment Completed

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1261322
UMLS CUI [1,2]
C2709094
UMLS CUI [1,3]
C0205197
prior concurrent therapy:
Beskrivning

Therapeutic procedure

Datatyp

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Beskrivning

ID.15

Datatyp

boolean

more than 1 week since prior chemotherapy or chemoradiation therapy
Beskrivning

Prior Chemotherapy | Chemoradiotherapy Previous

Datatyp

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2,1]
C0436307
UMLS CUI [2,2]
C0205156
no concurrent chemotherapy
Beskrivning

Exclusion Chemotherapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0392920
no other concurrent antineoplastic therapy (including standard-fractionated radiotherapy to the chest, chemotherapy, biological therapy, vaccine therapy, and surgery) 1 week before, during, and for 1 week after completion of study therapy
Beskrivning

Exclusion Criteria | Antineoplastic Drug/Agent Therapy | Therapeutic radiology procedure Chest | Chemotherapy | Biological treatment | Vaccine Therapy | Operative Surgical Procedures

Datatyp

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2]
C2346834
UMLS CUI [3,1]
C1522449
UMLS CUI [3,2]
C0817096
UMLS CUI [4]
C0392920
UMLS CUI [5]
C1531518
UMLS CUI [6]
C0042209
UMLS CUI [7]
C0543467
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Similar models

Eligibility Lung Cancer NCT00986297

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Non-Small Cell Lung Carcinoma
Item
histologically or cytologically confirmed non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
TNM clinical staging | Recurrent disease
Item
stage ii-iv and/or recurrent disease
boolean
C3258246 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
Exclusion Cell Small Histology
Item
no small cell histology
boolean
C2828389 (UMLS CUI [1,1])
C0007634 (UMLS CUI [1,2])
C0700321 (UMLS CUI [1,3])
C4048239 (UMLS CUI [1,4])
Measurable Disease | Evaluable Disease
Item
measurable or evaluable disease
boolean
C1513041 (UMLS CUI [1])
C1516986 (UMLS CUI [2])
Tumor Excision Unsuccessful
Item
tumor not amenable to surgical resection
boolean
C0027651 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Tumor Ineligible Stereotactic Body Radiotherapy
Item
tumor not eligible for stereotactic body radiation therapy
boolean
C0027651 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C1720823 (UMLS CUI [1,3])
Exclusion Criteria | Prior radiation therapy Region Neoplasm Involved | Overlap Radiation Field Current
Item
no prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields
boolean
C0680251 (UMLS CUI [1])
C0279134 (UMLS CUI [2,1])
C0205147 (UMLS CUI [2,2])
C0027651 (UMLS CUI [2,3])
C1314939 (UMLS CUI [2,4])
C1948020 (UMLS CUI [3,1])
C1882536 (UMLS CUI [3,2])
C0521116 (UMLS CUI [3,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Zubrod Performance Status
Item
zubrod performance status 2-4
boolean
C3714786 (UMLS CUI [1])
Pregnancy Absent | Breast Feeding Absent
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Pregnancy test negative
Item
negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must agree to use effective contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Evaluation pre treatment Completed
Item
must complete all required pretreatment evaluations
boolean
C1261322 (UMLS CUI [1,1])
C2709094 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.15
Item
see disease characteristics
boolean
Prior Chemotherapy | Chemoradiotherapy Previous
Item
more than 1 week since prior chemotherapy or chemoradiation therapy
boolean
C1514457 (UMLS CUI [1])
C0436307 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Exclusion Chemotherapy
Item
no concurrent chemotherapy
boolean
C2828389 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Exclusion Criteria | Antineoplastic Drug/Agent Therapy | Therapeutic radiology procedure Chest | Chemotherapy | Biological treatment | Vaccine Therapy | Operative Surgical Procedures
Item
no other concurrent antineoplastic therapy (including standard-fractionated radiotherapy to the chest, chemotherapy, biological therapy, vaccine therapy, and surgery) 1 week before, during, and for 1 week after completion of study therapy
boolean
C0680251 (UMLS CUI [1])
C2346834 (UMLS CUI [2])
C1522449 (UMLS CUI [3,1])
C0817096 (UMLS CUI [3,2])
C0392920 (UMLS CUI [4])
C1531518 (UMLS CUI [5])
C0042209 (UMLS CUI [6])
C0543467 (UMLS CUI [7])
Tillbaka till toppen 

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