Information:
Error:
ID
16476
Description
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
Keywords
Versions (1)
- 7/18/16 7/18/16 -
Uploaded on
July 18, 2016
DOI
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License
Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT00123799
Eligibility Breast Neoplasms NCT00123799
- StudyEvent: Eligibility
Similar models
Eligibility Breast Neoplasms NCT00123799
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
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])
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])
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])
Pregnancy | Breast Feeding
Item
nursing or pregnant females
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
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])
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])