Cryocompression for CIPN

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDana-Farber Cancer Institute

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

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators