Efficacy of Valproate in Peripheral Neuropathic Pain

Phase 2

Terminated

• Conditions: Neuralgia; Neuropathic Peripheral Pain

• Registration Number: NCT00221637
• Lead Sponsor: University Hospital, Bordeaux

Brief Summary

The purpose of this study is to determine whether valproate is effective and well tolerated in the treatment of neuropathic peripheral pain. The drug is administered by intravenous route followed by oral route during 4 weeks.

Detailed Description

Background. Neuropathic peripheral pain is often refractory to usual analgesics. Some anticonvulsant drugs may be effective, but often partially only, and not always well tolerated. Valproate is a well-known anticonvulsant drug, with moderate possible adverse events and for which an intravenous form is available.

Aim. The principal aim is to assess the efficacy and safety of sodium Valproate in peripheral neuropathic pain. Secondary aims are to asses the effect of IV and oral treatment on neurophysiologic measures.

Design. Randomized, double-blind vs. placebo, parallel groups, monocentric clinical trial.

Treatments. Experimental arm: Intravenous eight-hour sodium Valproate infusion, followed by a four-week oral route sodium Valproate treatment. Control arm: Intravenous eight-hour placebo infusion, followed by a four-week oral route placebo treatment. Rescue medications are allowed in both groups.

Eligibility criteria. Peripheral neuropathic pain with pain intensity of at least 40 mm on a visual analog scale.

Outcomes. Primary outcome is the intensity of pain on a visual analog scale after 4 weeks of treatment. Secondary outcomes: intensity of pain after IV treatment; neurophysiologic measures (thermal thresholds, RIII reflex); association of response to IV treatment with oral treatment efficacy.

Study Timeline

• Study Start: 2002-03
• Study Completion: 2005-07
• Study First Submitted: 2005-09-13
• Study First Submitted QC: 2005-09-13
• Study First Posted: 2005-09-22
• Status Verified: 2007-06
• Last Update Submitted: 2007-06-12
• Last Update Posted: 2007-06-13

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• peripheral neuropathic pain
• signed written informed consent

Exclusion Criteria

• central neuropathic pain
• current or past hepatic disease

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Intensity of pain on a visual analog scale	after 4 weeks of treatment

Secondary Outcome Measures

Name	Time	Method
intensity of mechanic allodynia
intensity of dynamic allodynia
use of analgesics (rescue medication)
thermal sensitive and nociceptive thresholds, RIII reflex

Trial Locations

Locations (1)

Unité de traitement de la douleur chronique, Hôpital Pellegrin, CHU de Bordeaux; 🇫🇷 Bordeaux, France