Breast Carcinoma TNM Breast tumor staging | Carcinoma in Situ TNM Breast tumor staging | LCIS TNM Breast tumor staging | DCIS TNM Breast tumor staging
Item
newly diagnosed stage i to iii breast cancer and carcinoma in situ (including lobular carcinoma in situ [lcis] and ductal carcinoma in situ [dcis])
boolean
C0678222 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
C0007099 (UMLS CUI [2,1])
C0474926 (UMLS CUI [2,2])
C0279563 (UMLS CUI [3,1])
C0474926 (UMLS CUI [3,2])
C0007124 (UMLS CUI [4,1])
C0474926 (UMLS CUI [4,2])
Operation on breast Planned | Segmental Mastectomy Planned | Mastectomy Planned
Item
breast surgery (lumpectomy or mastectomy) is planned for at least 7 days from the day of enrollment
boolean
C3714726 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0024885 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0024881 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
Informed Consent
Item
ability to understand and the willingness to sign an institutional review board (irb)-approved written informed consent document
boolean
C0021430 (UMLS CUI [1])
Tumor size Imaging | Tumor size Physical Examination
Item
tumor measures at least 1 centimeter on imaging or physical exam
boolean
C0475440 (UMLS CUI [1,1])
C0011923 (UMLS CUI [1,2])
C0475440 (UMLS CUI [2,1])
C0031809 (UMLS CUI [2,2])
Patient scheduled for surgery | Status post Biopsy
Item
any patient with surgery scheduled < 7days after biopsy
boolean
C3242215 (UMLS CUI [1])
C0231290 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
Discontinue NSAIDs Unable | Discontinue Aspirin Unable
Item
patients who are unable to refrain from the use of any nsaid or full-dose acetylsalicylic acid (asa)-containing nsaid while taking study drug
boolean
C1444662 (UMLS CUI [1,1])
C0003211 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1444662 (UMLS CUI [2,1])
C0004057 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
Neoadjuvant Chemotherapy
Item
patients who will receive neoadjuvant chemotherapy are not eligible
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
Omega-3 Fatty Acids
Item
patients who are currently taking omega-3 fatty acids, as they are unable to be randomized to placebo
boolean
C0015689 (UMLS CUI [1])
Omega-3 Fatty Acids Previous
Item
patients who have previously taken omega-3 fatty acid within 1 month prior to study enrollment
boolean
C0015689 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Allergy to fish
Item
patients with an allergy or known hypersensitivity to fish
boolean
C0856904 (UMLS CUI [1])