ID

16476

Descrição

Study of Fluorodeoxyglucose (FluGlucoScan) in Patients With Breast Cancer: Correlation With Histologic Findings of Sentinel Node Biopsies and Axillary Dissection; ODM derived from: https://clinicaltrials.gov/show/NCT00123799

Link

https://clinicaltrials.gov/show/NCT00123799

Palavras-chave

  1. 18/07/2016 18/07/2016 -
Transferido a

18 de julho de 2016

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Breast Neoplasms NCT00123799

Eligibility Breast Neoplasms NCT00123799

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female. if female of child bearing potential and outside of the window of 10 days since the last menstrual period, a negative pregnancy test.
Descrição

Gender | Childbearing Potential Pregnancy test negative | Date of last menstrual period

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0427780
UMLS CUI [3]
C0425932
biopsy proven breast carcinoma (core biopsy or fine needle aspiration, although core biopsies are preferred.)
Descrição

Breast Carcinoma | Core biopsy | Fine needle aspiration biopsy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C1318309
UMLS CUI [3]
C1510483
tumour size t1-3, n0 clinically
Descrição

Tumor size | TNM clinical staging

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0475440
UMLS CUI [2]
C3258246
all patients will have pre-operative mammography +/- ultrasound of the breast
Descrição

Mammography Preoperative | Ultrasonography, Mammary Preoperative

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C0445204
UMLS CUI [2,1]
C0080264
UMLS CUI [2,2]
C0445204
age equal to or greater than 18 years
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
able and willing to follow instructions and comply with the protocol
Descrição

Study Protocol Compliance behavior Willing

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C0600109
provide written informed consent prior to participation in this study
Descrição

Informed consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
nursing or pregnant females
Descrição

Pregnancy | Breast Feeding

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
previous malignancy or diagnosis less than 10 (ten) years ago. skin cancers (excluding malignant melanoma) and carcinoma in situ of the cervix are exceptions.
Descrição

Malignant Neoplasms | Skin carcinoma | melanoma | Carcinoma in situ of uterine cervix

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0699893
UMLS CUI [3]
C0025202
UMLS CUI [4]
C0851140
excisional biopsy of the tumour has been performed
Descrição

Excision biopsy Neoplasm

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0184921
UMLS CUI [1,2]
C0027651
age less than 18 years
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
patient has diabetes
Descrição

Diabetes Mellitus

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0011849

Similar models

Eligibility Breast Neoplasms NCT00123799

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Childbearing Potential Pregnancy test negative | Date of last menstrual period
Item
male or female. if female of child bearing potential and outside of the window of 10 days since the last menstrual period, a negative pregnancy test.
boolean
C0079399 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0427780 (UMLS CUI [2,2])
C0425932 (UMLS CUI [3])
Breast Carcinoma | Core biopsy | Fine needle aspiration biopsy
Item
biopsy proven breast carcinoma (core biopsy or fine needle aspiration, although core biopsies are preferred.)
boolean
C0678222 (UMLS CUI [1])
C1318309 (UMLS CUI [2])
C1510483 (UMLS CUI [3])
Tumor size | TNM clinical staging
Item
tumour size t1-3, n0 clinically
boolean
C0475440 (UMLS CUI [1])
C3258246 (UMLS CUI [2])
Mammography Preoperative | Ultrasonography, Mammary Preoperative
Item
all patients will have pre-operative mammography +/- ultrasound of the breast
boolean
C0024671 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C0080264 (UMLS CUI [2,1])
C0445204 (UMLS CUI [2,2])
Age
Item
age equal to or greater than 18 years
boolean
C0001779 (UMLS CUI [1])
Study Protocol Compliance behavior Willing
Item
able and willing to follow instructions and comply with the protocol
boolean
C2348563 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Informed consent
Item
provide written informed consent prior to participation in this study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
nursing or pregnant females
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Malignant Neoplasms | Skin carcinoma | melanoma | Carcinoma in situ of uterine cervix
Item
previous malignancy or diagnosis less than 10 (ten) years ago. skin cancers (excluding malignant melanoma) and carcinoma in situ of the cervix are exceptions.
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
C0025202 (UMLS CUI [3])
C0851140 (UMLS CUI [4])
Excision biopsy Neoplasm
Item
excisional biopsy of the tumour has been performed
boolean
C0184921 (UMLS CUI [1,1])
C0027651 (UMLS CUI [1,2])
Age
Item
age less than 18 years
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus
Item
patient has diabetes
boolean
C0011849 (UMLS CUI [1])

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