About this trial
This study aims to evaluate the effectiveness, tolerability, and safety of using cooling therapy and pressure (cryocompression) to reduce peripheral neuropathy, a condition affecting the nerves supplying the arms and legs (limbs) resulting in possible numbness, pain, and/or loss of motor function, that may occur as a result of taxane-based chemotherapy.
The name of the device used in this research study is:
-Paxman Limb Cryocompression System (PLCS)
Eligibility criteria
Qualifiers
Adults > 18 years of age
Gynecologic or breast malignancy
Weekly paclitaxel x 12 or weekly paclitaxel/carboplatin x 12, Q2 weeks paclitaxel X4 (preceded by doxorubicin/cyclophosphamide). (Breast Oncology)
Q3 weeks paclitaxel/carboplatin X 6-8 (GYN)
Disqualifiers
Previous exposure to neurotoxic chemotherapy
Pre-existing neuropathy
History of Raynaud's phenomenon, cold agglutinin disease, cryoglobulinemia, cryofibrinogenemia, post-traumatic cold dystrophy, peripheral arterial ischemia, or sickle cell disease
Undergoing desensitization
Trial design
Treatments tested in this trial
- Paxman Limb Cryocompression System