Unspecified Adult Solid Tumor, Protocol Specific Clinical Trial
Official title:
Placebo-Controlled Therapeutic Trial for the Prevention of Lymphedema in High Risk Patients
This randomized clinical trial studies an investigational drug in preventing lymphedema in patients at high risk after undergoing axillary lymph node dissection. The study drug may prevent lymphedema in patients undergoing axillary lymph node dissection.
PRIMARY OBJECTIVES:
I. To evaluate the efficacy of study drug in improving chronic lymphedema while further
elucidating the role of inflammatory and lymphangiogenic processes in the pathogenesis of
this disease.
OUTLINE: Patients are randomized to 1 of 2 treatment arms.
ARM I: Patients receive study drug orally (PO) thrice daily (TID) for up to 1 year in the
absence of disease progression or unacceptable toxicity.
ARM II: Patients receive placebo PO TID for up to 1 year in the absence of disease
progression or unacceptable toxicity.
After completion of study treatment, patients are followed up for 5 years.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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