The Effect of Oral Administration of Hesperidin and Diosmin in Reducing Paclitaxel-induced Peripheral Neuropathy in Breast Cancer Patients

Last updated: February 2, 2025
Sponsor: Alexandria University
Overall Status: Active - Not Recruiting

Phase

3

Condition

Breast Cancer

Cancer

Neurologic Disorders

Treatment

Hespiridin and Diosmin

Clinical Study ID

NCT06811220
0108808
  • Ages > 18
  • Female

Study Summary

The aim of this study is evaluation of the potential neuroprotective effect of oral hesperidin and diosmin in reducing paclitaxel- induced peripheral neuropathy in the treatment of breast cancer patients.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Female patients over 18 years of age with pathologically confirmed breast cancer.

  2. Breast cancer patients candidate for chemotherapy and will receive paclitaxel.

  3. Patients having an eastern cooperative oncology group (ECOG) score more than 2

Exclusion

Exclusion Criteria:

  1. Patients with signs and symptoms of clinical neuropathy at baseline.

  2. Patients with diabetes mellitus, alcoholic disease, heart failure, pregnant orlactating women.

  3. Patients receiving vitamin/ supplementation drugs that interfere with the studyintervention.

  4. Patients who have previously received chemotherapy.

  5. Hepatic impaired patients.

  6. Patient with history of allergy to hesperidin.

  7. Patients with history of allergy to diosmin.

  8. Renal impaired patients.

  9. Patient inadherent to paclitaxel.

  10. Patients inadherent to the administered hesperidin and diosmin during the studyperiod.

Study Design

Total Participants: 140
Treatment Group(s): 1
Primary Treatment: Hespiridin and Diosmin
Phase: 3
Study Start date:
January 27, 2025
Estimated Completion Date:
December 31, 2027