Gender | Age
Item
female, age 18 or older
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Breast Carcinoma
Item
diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
Breast Intact
Item
intact breast (not surgically absent)
boolean
C0006141 (UMLS CUI [1,1])
C0205266 (UMLS CUI [1,2])
Teleradiotherapy Fractionated
Item
planned fractionated external beam radiotherapy to be delivered by opposing, tangential beams to 50.4 gy in 28 fractions with a planned photon or electron boost of 10gy in 5 fractions (for a total of 33 fractions)
boolean
C0419095 (UMLS CUI [1,1])
C1979893 (UMLS CUI [1,2])
Comprehension Study Protocol | Protocol Compliance
Item
ability to understand and comply with the requirements of this study
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Informed Consent
Item
ability to give informed consent
boolean
C0021430 (UMLS CUI [1])
Gender Sexually active Contraceptive methods
Item
for sexually active females, patient agrees to use acceptable method of birth control
boolean
C0079399 (UMLS CUI [1,1])
C0241028 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
women who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Skin Care Preparations Portal triad area
Item
use of concomitant skin care preparations at any of the treated or control portal areas to be observed
boolean
C0150773 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0734842 (UMLS CUI [1,3])
Communicable Disease Therapeutic radiology procedure Portal triad area | Non-healed wound Therapeutic radiology procedure Portal triad area | Generalized dermatitis
Item
any infection or unhealed wound of the radiotherapy portal areas, or generalized dermatitis
boolean
C0009450 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C0734842 (UMLS CUI [1,3])
C0750433 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
C0734842 (UMLS CUI [2,3])
C0262995 (UMLS CUI [3])
Kidney Failure Severe | Creatinine measurement, serum
Item
severe renal failure creatinine > 3.0 within 6 months of study registration
boolean
C0035078 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0201976 (UMLS CUI [2])
Patient allergic history | Anaphylaxis | Severe allergy Investigational New Drugs | Severe allergy Placebo products
Item
allergic history, including anaphylaxis or severe allergies to products in study serum or placebo
boolean
C3841443 (UMLS CUI [1])
C0002792 (UMLS CUI [2])
C2945656 (UMLS CUI [3,1])
C0013230 (UMLS CUI [3,2])
C2945656 (UMLS CUI [4,1])
C1696465 (UMLS CUI [4,2])
C1514468 (UMLS CUI [4,3])
Relocation of home Planned | Follow-up visit Unsuccessful
Item
planned relocation which would make follow-up visits impossible during the course of the study
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0589121 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Collagen-vascular disease | Lupus Erythematosus | Scleroderma
Item
collagen vascular disease such as lupus, or scleroderma
boolean
C0262428 (UMLS CUI [1])
C0409974 (UMLS CUI [2])
C0011644 (UMLS CUI [3])