Topical Menthol Application in Chemotherapy-Related Peripheral Neuropathy in Patients With Breast Cancer
Breast Cancer, Peripheral Neuropathies, Chemotherapy Effect
About this trial
This is an interventional supportive care trial for Breast Cancer focused on measuring Breast Cancer, Peripheral neuropathy, Menthol, Chemotherapy
Eligibility Criteria
Inclusion Criteria:
- Patients who received at least two cycles of chemotherapy
- Patients aged 18 and over
- Women who received the paclitaxel chemotherapy protocol will be included.
Exclusion Criteria:
- Those with open wounds and edema on their hands and feet
- Patients with diabetes mellitus and peripheral neuropathy due to autoimmune disease
- Use complementary and alternative treatment methods to prevent peripheral neuropathy throughout the treatment process.
- Those who are allergic to topical menthol to be used in the study will be excluded from the study.
Sites / Locations
- Necmettin Erbakan University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Experimental
control group
During the study, the patients' routine pharmacological treatments will continue and menthol will be applied only to reduce the effect of neuropathy. In the study, menthol 1% will be used topically, as it was used in studies after the literature review. Although it was stated in the studies that menthol had no side effects, it was decided to mix menthol with water-based cream according to the literature recommendation. Researchers will first determine how many grams of menthol will be sufficient by applying menthol to their hands and feet.After the gram of the prepared mixture is determined, it will be given to the patients. Patients in the intervention group will be taught how to regularly apply menthol cream (topical menthol) to their hands and feet, twice a day, every day. The effect on CIPN will be evaluated in patients with CIPN for 3 weeks immediately before and after 6 weeks of treatment with menthol administration.
control group will receive standard practice