Clinical Trials Directory

Trials / Terminated

TerminatedNCT01911377

Botulinum Toxin Type A for Treating Allodynic Pain in SCI and MS

The Efficacy of Botulinum Toxin Type A in the Treatment of Allodynic-Type Neuropathic Pain in People With Spinal Cord Injury or Multiple Sclerosis

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
12 (actual)
Sponsor
University of Manitoba · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This study will examine the efficacy of Botulinum Toxin Type A ("Botox") in treating Allodynic-type neuropathic pain in people with spinal cord injury or multiple sclerosis. Neuropathic pain is pain initiated or caused by injury to or disease of the nervous system, and is common in spinal cord injury patients or people with multiple sclerosis. Allodynia is a type of neuropathic pain caused by something that normally would not cause pain, such as light touch, pressure from clothing, or bed sheets brushing against the skin. Botox has been used to treat the muscle overactivity that causes spasticity in spinal cord injured patients. It has been noticed to exert some analgesic(pain relieving) effect, and has recently been studied as a treatment for neuropathic pain. We want to see if Botox, injected intradermally, will relieve the symptoms of allodynic-type neuropathic pain. 24 volunteers are to be enrolled, with 16 receiving active treatment, and 8 "controls" receiving placebo.

Conditions

Interventions

TypeNameDescription
DRUGBotulinum Toxin Type A
DRUGNormal Saline for Injection

Timeline

Start date
2013-10-01
Primary completion
2015-05-01
Completion
2015-08-01
First posted
2013-07-30
Last updated
2015-10-02

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01911377. Inclusion in this directory is not an endorsement.