Pycnogenol for the Treatment of Lymphedema of the Arm in Breast Cancer Survivors
Lymphedema, Breast, Cancer
About this trial
This is an interventional treatment trial for Lymphedema focused on measuring lymphedema, breast, cancer, plant preparation, herbal preparation, pine bark extract
Eligibility Criteria
Inclusion criteria: Unilateral (ipsilateral to breast cancer resection side) lymphedema of the upper extremity. Extravascular water ration of > 1.07/1 between affected vs. normal arm using multiple frequency bioelectric impedence Patient is > 2months from last surgical or radiation treatment to the affected axilla Renal and hepatic function: Creatinine clearance > 50ml/min, total bili <2 mg/dl, transaminases <1.5 x ULN Patient not pregnant or breastfeeding. Use of barrier contraception if sexually active. ECOG performance of 0-2 Patient not allergic to pycnogenol Exclusion criteria: Patients treated with their first course of chemotherapy or radiation Chemotherapy or radiation to axillary lymph node will exclude patients for 8 weeks following treatment Patients with more than one episode of arm cellulitis, venous clot, or woody fibrosis of the affected arm. Antibiotics used to treat cellulitis must be completed at least 4 weeks prior to initial screening Patients with a defibrillator Midazolam study only: Patients requiring or benefiting from supplemental oxygen, patients allergic to cherries
Sites / Locations
- University of Wisconsin Comprehensive Cancer Center and School of Pharmacy