Breast Carcinoma | Lymphedema Mild | Lymphedema Moderate
Item
histological diagnosis of breast cancer with mild to moderate lymphedema (minimum of 200 mls or 10% and maximum 40% increase in arm volume over the unaffected arm.)
boolean
C0678222 (UMLS CUI [1])
C0024236 (UMLS CUI [2,1])
C2945599 (UMLS CUI [2,2])
C0024236 (UMLS CUI [3,1])
C0205081 (UMLS CUI [3,2])
Cancer treatment Completed | Cancer treatment Adjuvant Completed | Exception Hormone Therapy
Item
completion of all primary and adjuvant cancer treatments (with exception of endocrine treatment) 1 month prior to randomization.
boolean
C0920425 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0920425 (UMLS CUI [2,1])
C1522673 (UMLS CUI [2,2])
C0205197 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0279025 (UMLS CUI [3,2])
Maintenance therapy Lymphedema
Item
in or entering upon the maintenance phase of lymphedema treatment.
boolean
C0677908 (UMLS CUI [1,1])
C0024236 (UMLS CUI [1,2])
Compression Sleeve Daytime
Item
have properly fitted day-time compression sleeve and agree to wear sleeve for the 12 hour per day standard of care period
boolean
C0728907 (UMLS CUI [1,1])
C0183336 (UMLS CUI [1,2])
C0332169 (UMLS CUI [1,3])
Absence Compression Night time
Item
no current use of night-time compression (one month wash-out period before trial entry)
boolean
C0332197 (UMLS CUI [1,1])
C0728907 (UMLS CUI [1,2])
C0240526 (UMLS CUI [1,3])
Local disease | Neoplasm Metastasis
Item
clinical or radiological evidence of active disease, either local or metastatic
boolean
C0277565 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
Lymphedema of arm Bilateral
Item
history or clinical diagnosis of bilateral arm lymphedema
boolean
C0730207 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
Medical contraindication Compression | Communicable Disease Untreated | Skin irritation | Exanthema | Thrombosis Arm Affected
Item
anyone for whom compression is contraindicated, such as those with untreated infections, skin irritations/rash, or thrombosis of the affected arm
boolean
C1301624 (UMLS CUI [1,1])
C0728907 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2,1])
C0332155 (UMLS CUI [2,2])
C0152030 (UMLS CUI [3])
C0015230 (UMLS CUI [4])
C0040053 (UMLS CUI [5,1])
C1140618 (UMLS CUI [5,2])
C0392760 (UMLS CUI [5,3])
Disease Serious Excludes Informed Consent | Mental disorder Excludes Informed Consent | Addictive Behavior Excludes Informed Consent | Disease Serious Excludes Protocol Compliance | Mental disorder Excludes Protocol Compliance | Addictive Behavior Excludes Protocol Compliance
Item
serious non-malignant disease or any disorder/circumstance (psychiatric or addictive disorder) which would preclude consent/adherence to the protocol
boolean
C0012634 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,4])
C0004936 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
C0085281 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])
C0012634 (UMLS CUI [4,1])
C0205404 (UMLS CUI [4,2])
C0332196 (UMLS CUI [4,3])
C0525058 (UMLS CUI [4,4])
C0004936 (UMLS CUI [5,1])
C0332196 (UMLS CUI [5,2])
C0525058 (UMLS CUI [5,3])
C0085281 (UMLS CUI [6,1])
C0332196 (UMLS CUI [6,2])
C0525058 (UMLS CUI [6,3])
Protocol Compliance Unable | Etiology Patient on vacation
Item
unable to comply with the protocol, measurement and follow-up schedule due to factors such as vacation during the study period
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C0422297 (UMLS CUI [2,2])