ID

33437

Description

Comparison Study of Sentinel Lymph Node Biopsy by Multimodal Method in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01856452

Link

https://clinicaltrials.gov/show/NCT01856452

Keywords

  1. 12/8/18 12/8/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

December 8, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Neoplasms NCT01856452

Eligibility Breast Neoplasms NCT01856452

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinically lymph node negative breast cancer patients
Description

Breast Carcinoma Lymph Node Negative

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0678034
consented patients with more than 20 years
Description

Informed Consent | Age

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of breast cancer
Description

Medical History Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0678222
locally advanced breast cancer and metastatic breast cancer
Description

Locally advanced breast cancer | Secondary malignant neoplasm of female breast

Data type

boolean

Alias
UMLS CUI [1]
C3495949
UMLS CUI [2]
C0346993
proven axillary lymph node metastasis
Description

AXILLARY LYMPH NODE METASTASIS

Data type

boolean

Alias
UMLS CUI [1]
C0741344
history of axillary excisional or incisional biopsy, or dissection
Description

Excision biopsy Axillary | Incisional biopsy Axillary | Axillary dissection

Data type

boolean

Alias
UMLS CUI [1,1]
C0184921
UMLS CUI [1,2]
C0004454
UMLS CUI [2,1]
C0184922
UMLS CUI [2,2]
C0004454
UMLS CUI [3]
C0193867
history of neoadjuvant chemotherapy
Description

Chemotherapy Neoadjuvant

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0600558
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
non-consented patients
Description

Informed Consent Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
younger than 20 years old
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779

Similar models

Eligibility Breast Neoplasms NCT01856452

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma Lymph Node Negative
Item
clinically lymph node negative breast cancer patients
boolean
C0678222 (UMLS CUI [1,1])
C0678034 (UMLS CUI [1,2])
Informed Consent | Age
Item
consented patients with more than 20 years
boolean
C0021430 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Medical History Breast Carcinoma
Item
history of breast cancer
boolean
C0262926 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Locally advanced breast cancer | Secondary malignant neoplasm of female breast
Item
locally advanced breast cancer and metastatic breast cancer
boolean
C3495949 (UMLS CUI [1])
C0346993 (UMLS CUI [2])
AXILLARY LYMPH NODE METASTASIS
Item
proven axillary lymph node metastasis
boolean
C0741344 (UMLS CUI [1])
Excision biopsy Axillary | Incisional biopsy Axillary | Axillary dissection
Item
history of axillary excisional or incisional biopsy, or dissection
boolean
C0184921 (UMLS CUI [1,1])
C0004454 (UMLS CUI [1,2])
C0184922 (UMLS CUI [2,1])
C0004454 (UMLS CUI [2,2])
C0193867 (UMLS CUI [3])
Chemotherapy Neoadjuvant
Item
history of neoadjuvant chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C0600558 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Informed Consent Lacking
Item
non-consented patients
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Age
Item
younger than 20 years old
boolean
C0001779 (UMLS CUI [1])

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