Study protocol for a multi-institutional, randomised, double-blinded, placebo-controlled phase III trial investigating additive efficacy of duloxetine for neuropathic cancer pain refractory to opioids and gabapentinoids: the DIRECT study.

ABSTRACT:

Introduction

Management of patients with cancer suffering from neuropathic pain refractory to opioids and gabapentinoids remains an important challenge. Duloxetine is one of the choices after first-line treatment fails. The efficacy of duloxetine has been reported in patients with non-cancer disease and in chemotherapy-induced peripheral neuropathy, but no randomised clinical trials have examined its effects on neuropathic cancer pain refractory to first-line treatment. The objective of this study is to assess the analgesic efficacy of duloxetine in patients suffering from neuropathic cancer pain refractory to opioids and gabapentinoids.

Methods and analysis

A multi-institutional, prospective, randomised, double-blind, placebo-controlled, two-parallel trial is planned. The i

SUBMITTER: Matsuoka H 

PROVIDER: S-EPMC5724096 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature