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NCT07191587Completed

A Controlled Clinical Trial Assessing the Efficacy of Vitamin B Prophylaxis in Attenuating Paclitaxel-induced Neuropathy and the Imperative Use of Gabapentin in Diabetic Ovarian Cancer Patients and the Potential Effect on Disease Response.

Vitamin B Prophylaxis Effect on Peripheral Neuropathy Induced in Ovarian Cancer Patients Receiving Paclitaxel Based Regimen.

Source: ClinicalTrials.gov · Last updated 25 Sept 2025

Brief summary (registry, in English)

The goal of this clinical trial is to learn if vitamin B prophylaxis is effective in attenuating chemotherapy-induced peripheral neuropathy in adult ovarian cancer patients. The main questions (primary outcomes) it aims to answer are: * The severity of chemotherapy-induced peripheral neuropathy in ovarian cancer patients undergoing a weekly paclitaxel-based regimen in the vitamin B prophylactic group versus non-prophylactic group. * Severity of chemotherapy-induced peripheral neuropathy in diabetic patients versus non-diabetic patients in both prophylactic and non-prophylactic groups. Participants will: Take drug oral vitamin B complex every day as prophylaxis for 6 months. Visit the clinic once every week for their weekly Paclitaxel regimen, checkups and tests. Keep a diary of their symptoms.

Status (registry)
Completed
Study type
Interventional
Enrollment
146 (actual)
First submitted
2 Sept 2025
Start date
1 Dec 2024
Primary completion date
30 Apr 2025
Lead sponsor
National Cancer Institute, Egypt
NCT number
NCT07191587

What you commit to

  • Study type: Interventional
  • Participants enrolled: 146
  • From 1 Dec 2024 to the primary completion date, 30 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Individuals under 18 years of age.

Other

  • Any patients with pre-existing peripheral neuropathy.

Who the study is looking for

  • Female patients with confirmed pathology of ovarian adenocarcinoma.
  • Aged 18 years or older.
  • Scheduled to receive a weekly paclitaxel-based chemotherapy regimen (80 mg/m²).

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Cancer Institute
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.