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
About this trial
This is an interventional treatment trial for Multiple Sclerosis
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
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
NCT ID
NCT01018485
First Posted
November 19, 2009
Last Updated
May 8, 2015
Sponsor
Melbourne Health
Collaborators
Eastern Health
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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