Cryocompression With or Without Cilostazol for the Prevention of Paclitaxel-induced Neuropathy in Patients With Gynecological Cancers

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorEmory University

About this trial

The phase II trial evaluates the effectiveness of cryocompression therapy alone or in combination with cilostazol in preventing paclitaxel-induced peripheral neuropathy (numbness, pain or tingling in the feet and hands) for patients with gynecologic cancers. Peripheral neuropathy is a common side effect of many chemotherapeutic agents, including paclitaxel. Paclitaxel is in a class of medications called antimicrotubule agents. It stops cancer cells from growing and dividing and may kill them. Cryocompression is a therapy that combines compression garments or dressings with cooling of the treated area. Cilostazol is in a class of medications called platelet-aggregation inhibitors (antiplatelet medications). It works by improving blood flow to the legs. Giving cilostazol together with cryocompression may be safe and tolerable in treating patients with gynecological cancers.

Eligibility criteria

Qualifiers

Age 18 years or older

Diagnosis of uterine, ovarian/fallopian tube/primary peritoneal, cervical, or vulvar cancer and planned chemotherapy regimen of 6-9 cycles of paclitaxel and carboplatin or cisplatin with or without VEGF inhibition, with or without immunotherapy, and with or without HER2-directed therapy

Eastern Cooperative Oncology Group performance status from 0 to 2

ARM C: Age 18 years or older

Disqualifiers

Any patient unable and/or unwilling to cooperate with all study protocols

Previous treatment with paclitaxel

Patients with baseline pre-chemotherapy neuropathy requiring pharmacologic treatment

Diabetes mellitus with hemoglobin A1c >7.0

Trial design

Treatments tested in this trial

  • Best Practice
  • Cilostazol
  • Cryocompression Therapy
  • Paclitaxel
  • Quality-of-Life Assessment

Treatment groups

70 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Emory University

Lead sponsor

National Cancer Institute (NCI)

Collaborator