Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01325090

Early Administration of Botox® in Neuropathic Pain Due to Thoracoscopy or Thoracotomy

Early Administration of Botulinum Toxin Type A (Botox®) in Neuropathic Pain Due to Thoracoscopy or Thoracotomy: a Randomized, Double Blind, Placebo Controlled Study

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University Hospital, Limoges · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Botulinum toxin type A has been reported to inhibit the release of various pain neurotransmitters (SP, CGRP, glutamate) responsible for neurogenic inflammation, a process that results from the sensitization of C-fiber nociceptors (peripheral sensitization). This action is probably responsible for the analgesic effect of botulinum toxin type A recently demonstrated in patients with neuropathic pain of peripheral origin.In those studies, patients had been suffering for years. The investigators can hypothesizes that earlier administration of Botox in the course of neuropathic pain might prevent central sensitization, that is secondary to peripheral sensitization. The investigators can hope to increase efficacy of Botulinum toxin type A injections and to prevent chronification of pain.

Conditions

Interventions

TypeNameDescription
DRUGBOTOXA syringe of 1 ml contain 25 Allergan units.
OTHERPLACEBOThe pharmacist will fill syringes in tuberculins of 1 ml with injectable solution of sodium chloride of 0,9 %.

Timeline

Start date
2011-05-01
Primary completion
2013-11-01
Completion
2014-11-01
First posted
2011-03-29
Last updated
2018-08-13

Source: ClinicalTrials.gov record NCT01325090. Inclusion in this directory is not an endorsement.