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Recruiting Phase 2 NCT06492070

NCT06492070 Cryocompression With or Without Cilostazol for the Prevention of Paclitaxel-induced Neuropathy in Patients With Gynecological Cancers

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Clinical Trial Summary
NCT ID NCT06492070
Status Recruiting
Phase Phase 2
Sponsor Emory University
Condition Cervical Carcinoma
Study Type INTERVENTIONAL
Enrollment 70 participants
Start Date 2024-08-01
Primary Completion 2026-12-31

Trial Parameters

Condition Cervical Carcinoma
Sponsor Emory University
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 70
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2024-08-01
Completion 2026-12-31
Interventions
Best PracticeCilostazolCryocompression Therapy

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Brief Summary

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

Inclusion Criteria: * INCLUSION CRITERIA FOR ARMS A and B: * 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 * ARM C: Diagnosis of uterine, ovarian/fallopian tube/primary peritoneal, cervical, or vulvar cancer and completion of 6-9 cycles of a chemotherapy regimen consisting of paclitaxel and carboplatin or cisplatin with or without VEGF inhibition, with or without immunotherapy, and with or without HER2-directed therapy within the last 3 months * ARM C: Eastern Cooperative Oncology Group performance status from 0 to 2 Exclusion Criteria: * EXCLUSION CRITERIA FOR ARMS A and B: * Any patient unable and/or unwilling to cooperate wi

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