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Completed

NCT Number: NCT00444886

Treatment of Thoracic Outlet Syndrome (TOS) With Botox

The purpose of this study is:

1. To assess the effect of BOTOX injection to the scalene muscles on the severity of pain from TOS. 2. To assess the effect of BOTOX injection on numbness and tingling and quality of life.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

GF Strong Rehabilitation Centre

Vancouver, British Columbia, V5Z 2G9, Canada

About this study

Background:

Thoracic Outlet Syndrome (TOS) is a symptom complex consisting of pain, paresthesias and often functional impairment caused by compression of the neurovascular supply to the upper limb. Impingement may occur at the interscalene triangle, and both anesthetic blockade and chemodenervation of the scalene muscles have been shown to temporarily improve symptoms of TOS in non-randomized controlled trials.

Objective:

To assess the effect of Botulinum Toxin Type A (BTX-A) injections into the scalene muscles on pain, paresthesias and function in subjects with TOS.

Hypothesis:

BTX-A injected into the anterior and middle scalene muscles will reduce the irritation on the neurovascular structures at the interscalene triangle in subjects with TOS. This will lead to reductions in pain and paresthesias, and improvements in function when compared with injection of placebo.

Intervention:

Each subject will receive an injection under EMG guidance into the anterior and middle scalene muscles of either 75 units of BTX-A (experimental group), or normal saline (control group). Both groups will be provided with a stretching and strengthening exercise program.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age at least 19 years
  • Medically stable
  • Able to give informed consent
  • Meets criteria for clinical diagnosis of TOS
  • Symptoms of TOS present for at least six months
  • Have had EMG studies and a CT or MRI scan of the cervical spine

Exclusion criteria

  • Prior treatment with BTX-A
  • Allergy to BTX-A
  • History of botulinum toxicity
  • Prior scalenectomy
  • Surgery for TOS planned within six months
  • Use of blood thinners, i.e., warfarin; unfractionated or low molecular weight heparin
  • History of Myasthenia Gravis, Eaton-Lambert Syndrome or Shy-Drager Syndrome
  • Unable to complete follow-up assessments at 6 weeks, 3 months and 6 months
  • Any abnormalities on EMG, CT or MRI studies suggesting an alternate diagnosis
  • Pregnancy or planned pregnancy within six months

Treatment and study plan

Botulinum Toxin Type A injection (BOTOX)

Drug

Each subject will receive an injection under EMG guidance into the anterior and middle scalene muscles of either 75 units of BTX-A (experimental group), or normal saline (control group). Both groups will be provided with a stretching and strengthening exercise program.

Primary outcomes

  1. Pain as measured on Visual Analog Scale (VAS) at 6 weeks, 3 months and 6 months post-intervention

    Time frame: 6 monhts

Secondary outcomes

  1. Paresthesias as measured on VAS

    Time frame: 6 months

  2. Function as measured with Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire, SF-36, number of days lost from work

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

University of British Columbia

Other

Collaborators

  • Allergan

Registry information

Official study title

Treatment of Thoracic Outlet Syndrome With Botulinum Toxin Injection: A Double-Blind, Randomized Controlled Trial

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Mar 8, 2007
Registry last updated
Feb 10, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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