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Eligibility Breast Cancer NCT00594477

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female gender
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
age ≥ 18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
invasive primary female breast cancer
Description

Invasive carcinoma of breast Primary

Type de données

boolean

Alias
UMLS CUI [1,1]
C0853879
UMLS CUI [1,2]
C0205225
pathologically proven regional nodal metastasis
Description

Secondary malignant neoplasm of lymph node regional

Type de données

boolean

Alias
UMLS CUI [1,1]
C0686619
UMLS CUI [1,2]
C0205147
status post mastectomy or partial mastectomy with an assessment of axillary nodes via sentinel lymph node biopsy and/or axillary lymph node dissection.
Description

Mastectomy Status post | Segmental Mastectomy Status post | Axillary lymph nodes Assessment Sentinel Lymph Node Biopsy | Excision of axillary lymph nodes

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024881
UMLS CUI [1,2]
C0231290
UMLS CUI [2,1]
C0024885
UMLS CUI [2,2]
C0231290
UMLS CUI [3,1]
C0729594
UMLS CUI [3,2]
C1516048
UMLS CUI [3,3]
C0796693
UMLS CUI [4]
C0193867
signed study specific consent form
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
distant metastasis
Description

Distant metastasis

Type de données

boolean

Alias
UMLS CUI [1]
C1275402
currently pregnant
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
psychiatric or addictive disorders that preclude informed consent
Description

Mental disorders Exclude Informed Consent | Addictive Behavior Excludes Informed Consent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0021430
UMLS CUI [2,1]
C0085281
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C0021430
time from initial diagnosis to the start of radiation therapy > one year
Description

Time Interval Initial diagnosis Start Therapeutic radiology procedure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0872291
UMLS CUI [1,2]
C4071762
UMLS CUI [1,3]
C0439659
UMLS CUI [1,4]
C1522449
estimated life expectancy judged to be < one year
Description

Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
prior radiation to the ipsilateral breast or chest wall
Description

Prior radiation therapy Breast Ipsilateral | Radiotherapy to chest wall

Type de données

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C0006141
UMLS CUI [1,3]
C0441989
UMLS CUI [2]
C1998066
primary breast cancer is lymphoma or sarcoma
Description

Breast Carcinoma Primary | Lymphoma | Sarcoma

Type de données

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205225
UMLS CUI [2]
C0024299
UMLS CUI [3]
C1261473
patients being treated with concurrent chemotherapy.
Description

Chemotherapy Concurrent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0205420
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Similar models

Eligibility Breast Cancer NCT00594477

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female gender
boolean
C0079399 (UMLS CUI [1])
Age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Invasive carcinoma of breast Primary
Item
invasive primary female breast cancer
boolean
C0853879 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Secondary malignant neoplasm of lymph node regional
Item
pathologically proven regional nodal metastasis
boolean
C0686619 (UMLS CUI [1,1])
C0205147 (UMLS CUI [1,2])
Mastectomy Status post | Segmental Mastectomy Status post | Axillary lymph nodes Assessment Sentinel Lymph Node Biopsy | Excision of axillary lymph nodes
Item
status post mastectomy or partial mastectomy with an assessment of axillary nodes via sentinel lymph node biopsy and/or axillary lymph node dissection.
boolean
C0024881 (UMLS CUI [1,1])
C0231290 (UMLS CUI [1,2])
C0024885 (UMLS CUI [2,1])
C0231290 (UMLS CUI [2,2])
C0729594 (UMLS CUI [3,1])
C1516048 (UMLS CUI [3,2])
C0796693 (UMLS CUI [3,3])
C0193867 (UMLS CUI [4])
Informed Consent
Item
signed study specific consent form
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Distant metastasis
Item
distant metastasis
boolean
C1275402 (UMLS CUI [1])
Pregnancy
Item
currently pregnant
boolean
C0032961 (UMLS CUI [1])
Mental disorders Exclude Informed Consent | Addictive Behavior Excludes Informed Consent
Item
psychiatric or addictive disorders that preclude informed consent
boolean
C0004936 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0085281 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
Time Interval Initial diagnosis Start Therapeutic radiology procedure
Item
time from initial diagnosis to the start of radiation therapy > one year
boolean
C0872291 (UMLS CUI [1,1])
C4071762 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
Life Expectancy
Item
estimated life expectancy judged to be < one year
boolean
C0023671 (UMLS CUI [1])
Prior radiation therapy Breast Ipsilateral | Radiotherapy to chest wall
Item
prior radiation to the ipsilateral breast or chest wall
boolean
C0279134 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,3])
C1998066 (UMLS CUI [2])
Breast Carcinoma Primary | Lymphoma | Sarcoma
Item
primary breast cancer is lymphoma or sarcoma
boolean
C0678222 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0024299 (UMLS CUI [2])
C1261473 (UMLS CUI [3])
Chemotherapy Concurrent
Item
patients being treated with concurrent chemotherapy.
boolean
C0392920 (UMLS CUI [1,1])
C0205420 (UMLS CUI [1,2])
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