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The Efficacy of Botulinum Toxin in Disabling Multiple Sclerosis (MS) Tremor

Primary Purpose

Multiple Sclerosis, Tremor

Status
Completed
Phase
Phase 3
Locations
Australia
Study Type
Interventional
Intervention
Botulinum Toxin Type A
Sponsored by
Melbourne Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Relapsing-remitting MS or secondary progressive MS according to the Mc Donald criteria
  • Age 18-80 years of age
  • Competent to understand and sign informed consent
  • Presence of symptomatic head and/or limb tremor

Exclusion Criteria:

  • Treatment with botulinum toxin type A of any brand within the 4 months prior to enrollment
  • A known contraindication to Botox injection
  • Pregnancy

Sites / Locations

  • Melbourne Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Botulinum Toxin First Dose

Botulinum Toxin Second Dose

Arm Description

Blinded and Randomized injection of 20 upper limbs with Botulinum Toxin Type A

20 patients will receive Placebo as first dose and Botulinum Toxin as second dose injection 3 months after initiation of the study

Outcomes

Primary Outcome Measures

A decrease in tremor

Secondary Outcome Measures

The safety profile of Botulinum Toxin in MS patients

Full Information

First Posted
November 19, 2009
Last Updated
May 8, 2015
Sponsor
Melbourne Health
Collaborators
Eastern Health
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1. Study Identification

Unique Protocol Identification Number
NCT01018485
Brief Title
The Efficacy of Botulinum Toxin in Disabling Multiple Sclerosis (MS) Tremor
Official Title
Double-Blind, Randomized, Controlled, Cross-over Comparison of Efficacy and Safety of Botulinum Toxin Type A in the Targeted Treatment of Disabling Tremor in Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Melbourne Health
Collaborators
Eastern Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The incidence of tremor in Multiple Sclerosis (MS) has been estimated to affect up to 2/3rds of patients. Over half of the tremors involve the upper limb and frequently lead to further disability. Medical treatment of MS tremor is generally unrewarding, although carbamazepine, clonazepam, glutethimide, hyoscine, isoniazid, ondansetron, primidone, and tetrahydrocannabinol have been reported to have some beneficial effect but published evidence of effectiveness is very limited. The investigators' experience to date suggests that many of the upper limb tremors may potentially be responsive to Botulinum toxin injection therapy. Aims: 1. The investigators aim to determine the efficacy of commonly used doses of BOTOX on the patients with symptomatic unilateral or bilateral arm tremor due to MS; and any side effects associated with this treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Tremor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Botulinum Toxin First Dose
Arm Type
Experimental
Arm Description
Blinded and Randomized injection of 20 upper limbs with Botulinum Toxin Type A
Arm Title
Botulinum Toxin Second Dose
Arm Type
Experimental
Arm Description
20 patients will receive Placebo as first dose and Botulinum Toxin as second dose injection 3 months after initiation of the study
Intervention Type
Drug
Intervention Name(s)
Botulinum Toxin Type A
Other Intervention Name(s)
Botox
Intervention Description
Intramuscular injection in affected limb up to 100 Units. Two doses (one placebo, one active) 3 months apart.
Primary Outcome Measure Information:
Title
A decrease in tremor
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The safety profile of Botulinum Toxin in MS patients
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Relapsing-remitting MS or secondary progressive MS according to the Mc Donald criteria Age 18-80 years of age Competent to understand and sign informed consent Presence of symptomatic head and/or limb tremor Exclusion Criteria: Treatment with botulinum toxin type A of any brand within the 4 months prior to enrollment A known contraindication to Botox injection Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Evans, MD
Organizational Affiliation
Melbourne Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Melbourne Health
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3050
Country
Australia

12. IPD Sharing Statement

Learn more about this trial

The Efficacy of Botulinum Toxin in Disabling Multiple Sclerosis (MS) Tremor

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