Gender | Age
Item
female aged between 40 and 60
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Noninfiltrating Intraductal Carcinoma | Tumor Stage Classification | Negative Surgical Margin Histopathologic examination
Item
subjects who diagnosed breast ductal carcinoma in situ of surgical staging t1an0, negative resection margin of below 2mm in histopathologic examination
boolean
C0007124 (UMLS CUI [1])
C0178759 (UMLS CUI [2])
C1709157 (UMLS CUI [3,1])
C0677043 (UMLS CUI [3,2])
Relapse | Interval | Breast-Conserving Surgery Breast Carcinoma | Therapeutic radiology procedure
Item
subjects who have a relapse-free interval of more than one year after breast-conserving surgery for breast cancer and radiation therapy
boolean
C0035020 (UMLS CUI [1])
C1272706 (UMLS CUI [2])
C0917927 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
C1522449 (UMLS CUI [4])
Comprehension Study Protocol | Informed Consent
Item
subjects who understand the study contents and sign the informed consent
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Radiodermatitis
Item
subjects who have radiodermatitis
boolean
C0034561 (UMLS CUI [1])
Breast reconstruction, bilateral, with bilateral TRAM free flaps Planned | Body tissue Autogenous
Item
subjects who planned breast reconstruction with autogenous tissue (ex.transverse rectus abdominis muscle flap)
boolean
C0521246 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0040300 (UMLS CUI [2,1])
C0443145 (UMLS CUI [2,2])
Smoking History
Item
subjects who have a history of smoking within 3months recently
boolean
C1519384 (UMLS CUI [1])
Study Subject Participation Status
Item
subjects who participated in other clinical trial within 30 days recently
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating subjects
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Communicable Diseases
Item
subjects who have a active infectious disease
boolean
C0009450 (UMLS CUI [1])
Eligibility Determination | clinical research investigator
Item
subjects who are not eligible for this study at the discretion of the investigator
boolean
C0013893 (UMLS CUI [1])
C1552025 (UMLS CUI [2])