Eligibility Breast Cancer NCT00820690

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
women with locally advanced women breast cancer
Description

Gender | Locally advanced breast cancer

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C3495949
histology: ductal ou lobular invasive histology
Description

Histology Ductal | Histology Invasive Lobular

Type de données

boolean

Alias
UMLS CUI [1,1]
C0344441
UMLS CUI [1,2]
C1512083
UMLS CUI [2,1]
C0344441
UMLS CUI [2,2]
C0205281
UMLS CUI [2,3]
C0205417
agreement to take part in the study and signature of the informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
clinical condition to receive doxorubicin/cyclophosphamide and paclitaxel
Description

Condition Clinical Receive Doxorubicin | Condition Clinical Receive Cyclophosphamide | Condition Clinical Receive Paclitaxel

Type de données

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0205210
UMLS CUI [1,3]
C1514756
UMLS CUI [1,4]
C0013089
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0205210
UMLS CUI [2,3]
C1514756
UMLS CUI [2,4]
C0010583
UMLS CUI [3,1]
C0348080
UMLS CUI [3,2]
C0205210
UMLS CUI [3,3]
C1514756
UMLS CUI [3,4]
C0144576
ecog 0 or i
Description

ECOG performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
not clinical stage iii
Description

TNM clinical staging

Type de données

boolean

Alias
UMLS CUI [1]
C3258246
inflammatory breast cancer
Description

Inflammatory Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0278601
previous treatment
Description

Prior Therapy

Type de données

boolean

Alias
UMLS CUI [1]
C1514463
previous diagnosis of cancer (except basal cell or squamous cell skin carcinoma and non-invasive cervical carcinoma)
Description

Malignant Neoplasms | Exception Basal cell carcinoma | Exception Squamous cell carcinoma of skin | Exception Cervix carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007117
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0553723
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0302592
pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
absence of clinical condition to receive chemotherapy
Description

Absence Condition Receive Chemotherapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0348080
UMLS CUI [1,3]
C1514756
UMLS CUI [1,4]
C0392920

Similar models

Eligibility Breast Cancer NCT00820690

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Locally advanced breast cancer
Item
women with locally advanced women breast cancer
boolean
C0079399 (UMLS CUI [1])
C3495949 (UMLS CUI [2])
Histology Ductal | Histology Invasive Lobular
Item
histology: ductal ou lobular invasive histology
boolean
C0344441 (UMLS CUI [1,1])
C1512083 (UMLS CUI [1,2])
C0344441 (UMLS CUI [2,1])
C0205281 (UMLS CUI [2,2])
C0205417 (UMLS CUI [2,3])
Informed Consent
Item
agreement to take part in the study and signature of the informed consent
boolean
C0021430 (UMLS CUI [1])
Condition Clinical Receive Doxorubicin | Condition Clinical Receive Cyclophosphamide | Condition Clinical Receive Paclitaxel
Item
clinical condition to receive doxorubicin/cyclophosphamide and paclitaxel
boolean
C0348080 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
C0013089 (UMLS CUI [1,4])
C0348080 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1514756 (UMLS CUI [2,3])
C0010583 (UMLS CUI [2,4])
C0348080 (UMLS CUI [3,1])
C0205210 (UMLS CUI [3,2])
C1514756 (UMLS CUI [3,3])
C0144576 (UMLS CUI [3,4])
ECOG performance status
Item
ecog 0 or i
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
TNM clinical staging
Item
not clinical stage iii
boolean
C3258246 (UMLS CUI [1])
Inflammatory Breast Carcinoma
Item
inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
Prior Therapy
Item
previous treatment
boolean
C1514463 (UMLS CUI [1])
Malignant Neoplasms | Exception Basal cell carcinoma | Exception Squamous cell carcinoma of skin | Exception Cervix carcinoma
Item
previous diagnosis of cancer (except basal cell or squamous cell skin carcinoma and non-invasive cervical carcinoma)
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0553723 (UMLS CUI [3,2])
C1705847 (UMLS CUI [4,1])
C0302592 (UMLS CUI [4,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Absence Condition Receive Chemotherapy
Item
absence of clinical condition to receive chemotherapy
boolean
C0332197 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
C0392920 (UMLS CUI [1,4])