ID

37859

Description

Excision Followed by Radiofrequency Ablation for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01153035

Link

https://clinicaltrials.gov/show/NCT01153035

Keywords

  1. 8/28/19 8/28/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

August 28, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01153035

Eligibility Breast Cancer NCT01153035

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient is a female, ≥ 50 years of age
Description

Gender | Age

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
the tumor size is ≤ 3 cm (on pre-study radiologic or clinical exam)
Description

Tumor size Diagnostic radiologic examination | Tumor size Clinical examination

Data type

boolean

Alias
UMLS CUI [1,1]
C0475440
UMLS CUI [1,2]
C0043299
UMLS CUI [2,1]
C0475440
UMLS CUI [2,2]
C1456356
the tumor is unicentric and unilateral
Description

Tumor Unicentric | Tumor Unilateral

Data type

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C4518564
UMLS CUI [2,1]
C0027651
UMLS CUI [2,2]
C0205092
the tumor is not involving the skin
Description

Tumor | Involvement with Skin Absent

Data type

boolean

Alias
UMLS CUI [1]
C0027651
UMLS CUI [2,1]
C1314939
UMLS CUI [2,2]
C1123023
UMLS CUI [2,3]
C0332197
pathology confirms ductal in situ (dcis) or infiltrating ductal carcinoma (idc), grade i-iii
Description

DCIS Grade | Infiltrating ductal carcinoma Grade

Data type

boolean

Alias
UMLS CUI [1,1]
C0007124
UMLS CUI [1,2]
C0441800
UMLS CUI [2,1]
C1134719
UMLS CUI [2,2]
C0441800
if tumor is idc, pathology must be hormone receptor positive (er+ and/or pr+)
Description

Invasive Ductal Breast Carcinoma Estrogen receptor positive | Invasive Ductal Breast Carcinoma Progesterone receptor positive

Data type

boolean

Alias
UMLS CUI [1,1]
C1134719
UMLS CUI [1,2]
C0279754
UMLS CUI [2,1]
C1134719
UMLS CUI [2,2]
C0279759
patient signs current written informed consent and hipaa forms
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient is under 50 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patient is male
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
tumor > 3 cm in diameter
Description

Tumor size Diameter

Data type

boolean

Alias
UMLS CUI [1,1]
C0475440
UMLS CUI [1,2]
C1301886
bilateral malignancy
Description

Bilateral Malignant Neoplasm

Data type

boolean

Alias
UMLS CUI [1]
C0677861
clinically positive lymph nodes
Description

Lymph node positive Clinical

Data type

boolean

Alias
UMLS CUI [1,1]
C0746319
UMLS CUI [1,2]
C0205210
tumor involving the skin
Description

Tumor Involving Skin

Data type

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C1123023
pathology confirms invasive lobular carcinoma
Description

Invasive Lobular Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0279565
breast implants
Description

Breast implants

Data type

boolean

Alias
UMLS CUI [1]
C0179412
less than 2 years disease-free survival from previous breast cancer
Description

Breast Carcinoma Previous | Disease Free Survival time

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205156
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0332296
UMLS CUI [2,3]
C2919552
neoadjuvant chemotherapy or chemotherapy for another breast cancer within two years
Description

Neoadjuvant Chemotherapy Breast Carcinoma Other | Chemotherapy Breast Carcinoma Other

Data type

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C3665472
UMLS CUI [1,3]
C0678222
UMLS CUI [1,4]
C0205394
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0678222
UMLS CUI [2,3]
C0205394

Similar models

Eligibility Breast Cancer NCT01153035

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
patient is a female, ≥ 50 years of age
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Tumor size Diagnostic radiologic examination | Tumor size Clinical examination
Item
the tumor size is ≤ 3 cm (on pre-study radiologic or clinical exam)
boolean
C0475440 (UMLS CUI [1,1])
C0043299 (UMLS CUI [1,2])
C0475440 (UMLS CUI [2,1])
C1456356 (UMLS CUI [2,2])
Tumor Unicentric | Tumor Unilateral
Item
the tumor is unicentric and unilateral
boolean
C0027651 (UMLS CUI [1,1])
C4518564 (UMLS CUI [1,2])
C0027651 (UMLS CUI [2,1])
C0205092 (UMLS CUI [2,2])
Tumor | Involvement with Skin Absent
Item
the tumor is not involving the skin
boolean
C0027651 (UMLS CUI [1])
C1314939 (UMLS CUI [2,1])
C1123023 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
DCIS Grade | Infiltrating ductal carcinoma Grade
Item
pathology confirms ductal in situ (dcis) or infiltrating ductal carcinoma (idc), grade i-iii
boolean
C0007124 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C1134719 (UMLS CUI [2,1])
C0441800 (UMLS CUI [2,2])
Invasive Ductal Breast Carcinoma Estrogen receptor positive | Invasive Ductal Breast Carcinoma Progesterone receptor positive
Item
if tumor is idc, pathology must be hormone receptor positive (er+ and/or pr+)
boolean
C1134719 (UMLS CUI [1,1])
C0279754 (UMLS CUI [1,2])
C1134719 (UMLS CUI [2,1])
C0279759 (UMLS CUI [2,2])
Informed Consent
Item
patient signs current written informed consent and hipaa forms
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
patient is under 50 years of age
boolean
C0001779 (UMLS CUI [1])
Gender
Item
patient is male
boolean
C0079399 (UMLS CUI [1])
Tumor size Diameter
Item
tumor > 3 cm in diameter
boolean
C0475440 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
Bilateral Malignant Neoplasm
Item
bilateral malignancy
boolean
C0677861 (UMLS CUI [1])
Lymph node positive Clinical
Item
clinically positive lymph nodes
boolean
C0746319 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
Tumor Involving Skin
Item
tumor involving the skin
boolean
C0027651 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C1123023 (UMLS CUI [1,3])
Invasive Lobular Carcinoma
Item
pathology confirms invasive lobular carcinoma
boolean
C0279565 (UMLS CUI [1])
Breast implants
Item
breast implants
boolean
C0179412 (UMLS CUI [1])
Breast Carcinoma Previous | Disease Free Survival time
Item
less than 2 years disease-free survival from previous breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2,1])
C0332296 (UMLS CUI [2,2])
C2919552 (UMLS CUI [2,3])
Neoadjuvant Chemotherapy Breast Carcinoma Other | Chemotherapy Breast Carcinoma Other
Item
neoadjuvant chemotherapy or chemotherapy for another breast cancer within two years
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C0392920 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C0205394 (UMLS CUI [2,3])

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