drugset / Trial / NCT04201561

High Dose Inorganic Selenium for Preventing Chemotherapy Induced Peripheral Neuropathy

NCT04201561 ↗

RandomizedParallel-groupTriple-blindPrevention

Summary

This study aims to evaluate the safety and efficacy of high dose inorganic selenium in preventing and relieving chemotherapy-induced peripheral neuropathy (CIPN) in platinum-sensitive recurrent ovarian, fallopian, or primary peritoneal cancer patients. This study will be conducted as a phase III randomized controlled trial in platinum-sensitive recurrent ovarian, fallopian, or primary peritoneal cancer patients who are expected to undergo paclitaxel-carboplatin chemotherapy. A total of 68 patients need to be enrolled in this study. The primary objective of this study is to evaluate the frequency of chemotherapy-induced peripheral neuropathy. The secondary objectives are the evaluation of the severity of peripheral neuropathy and the quality of life to show that selenium is effective in preventing and relieving peripheral neuropathy induced by paclitaxel. Positive results in this study will lead to further studies investigating the effect of selenium on other chemotherapies that can induce peripheral neuropathy.

Timeline

Start
2019-12-24
Primary completion
2023-04-30
Completion
2024-12-31

Outcome

Missed primary endpoint

paper While the primary endpoint was not met, selenium showed the potential of protective effects against motor neuropathy without safety and survival concerns. PMID 41630017 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject sodium selenite pentahydrate Unknown 2000 ug Intravenous
Background Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Background Carboplatin Small molecule — Intravenous
Background Paclitaxel Small molecule 175 mg/m2 Intravenous