ID

16476

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00123799

Nyckelord

  1. 2016-07-18 2016-07-18 -
Uppladdad den

18 juli 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Neoplasms NCT00123799

Eligibility Breast Neoplasms NCT00123799

Inclusion Criteria
Beskrivning

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.
Beskrivning

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

Datatyp

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.)
Beskrivning

Breast Carcinoma | Core biopsy | Fine needle aspiration biopsy

Datatyp

boolean

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

Tumor size | TNM clinical staging

Datatyp

boolean

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

Mammography Preoperative | Ultrasonography, Mammary Preoperative

Datatyp

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
Beskrivning

Age

Datatyp

boolean

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

Study Protocol Compliance behavior Willing

Datatyp

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
Beskrivning

Informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
nursing or pregnant females
Beskrivning

Pregnancy | Breast Feeding

Datatyp

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.
Beskrivning

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

Datatyp

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
Beskrivning

Excision biopsy Neoplasm

Datatyp

boolean

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

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
patient has diabetes
Beskrivning

Diabetes Mellitus

Datatyp

boolean

Alias
UMLS CUI [1]
C0011849

Similar models

Eligibility Breast Neoplasms NCT00123799

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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