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A Safety/Efficacy Trial of Zonisamide for Essential Tremor

Primary Purpose

Essential Tremor

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Zonisamide
Sponsored by
VA Greater Los Angeles Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Essential Tremor focused on measuring essential tremor, zonisamide, clinical trial

Eligibility Criteria

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

Inclusion Criteria: age 18 or older diagnosis of essential tremor tremor present in both hands for at least one year tremor is bothersome in at least one hand, so that reduction of tremor would improve quality of life able to comply with study visits and procedures has voluntarily signed consent form able to abstain from alcohol for 12 hours prior to each visit, and from caffeine on day prior to visit taking no medications or stable doses of anti-tremor medication for 4 weeks prior to the Baseline visit Exclusion Criteria: medical condition likely to cause hospitalization during the study progressive neurological disorder other than essential tremor history of serious psychiatric illness history of drug or alcohol abuse in past year consumes more than two glasses of wine or equivalent per day has received botulinum toxin injection in past 6 months currently using experimental device has taken experimental drug within 5 half lives of its elimination has received deep brain stimulation in past two weeks or has potential need for this therapy during the study thalamotomy within the past 6 months taking medications judged by investigator to exacerbate tremor has probable cause of tremor other than essential tremor condition likely to interfere with absorption, metabolism or elimination of study drug hepatic disease renal disease history of renal stones history of allergy to sulfonamides

Sites / Locations

  • VA Greater Los Angeles

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Zonisamide

Arm Description

Zonisamide administration and tremor assessment to assess efficacy in reducing essential tremor

Outcomes

Primary Outcome Measures

The degree of tremor at the end of the dose adjustment phase compared to baseline.

Secondary Outcome Measures

Quality of life.
Degree of tremor at the end of the extension phase compared to the beginning of the extension phase.

Full Information

First Posted
September 15, 2005
Last Updated
June 20, 2012
Sponsor
VA Greater Los Angeles Healthcare System
Collaborators
Ralph M. Parsons Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00223743
Brief Title
A Safety/Efficacy Trial of Zonisamide for Essential Tremor
Official Title
Novel Therapies for Essential Tremor - Zonisamide Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
November 2004 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
VA Greater Los Angeles Healthcare System
Collaborators
Ralph M. Parsons Foundation

4. Oversight

5. Study Description

Brief Summary
The purpose of this pilot study is to obtain information whether the medication zonisamide reduces tremor in persons with essential tremor and is well tolerated.
Detailed Description
Essential tremor is common, affecting about four percent of the population above age 40 years. Of these, about half have troublesome tremor that warrants medical therapy, but only half of these find satisfactory treatment. Thus it can be estimated that about one million Americans have not been able to find adequate therapy for their essential tremor. Presently used medications may fail due to lack of efficacy or tolerance. After encountering anecdotal experience of zonisamide's efficacy for essential tremor we decided to conduct a single-site open-treatment rising-dose study with blinded videotape ratings of tremor. Zonisamide is presently on the market in the United States for epilepsy. Its use in other conditions is experimental. Healthy participants with bilateral hand tremor will initially sign an IRB-approved informed consent form, then have assessments in a Screening Visit to determine that they are healthy (physical and neurological examinations, routine blood tests, electrocardiogram) and tremor assessments with rating scales. Tremor at each visit will be videotaped, as well as assessed openly by a rater. If participants meet eligibility criteria, they will return to a Baseline Visit (Visit 1) for repeat tremor assessment and the initial dispensation of zonisamide. The study drug initially will taken as one 50-mg tablet a day, then the dose increased by one tablet each two weeks, to no more than 3 tablets (150 mg) taken twice a day. During this 12-week dose adjustment phase, the participant will be seen in clinic each 4 weeks for tremor assessments and review of health status. In addition, the participant will be contacted by telephone each week. If any symptom occurs suggestive of side effects, the escalation will be stopped or the dose reduced in order to resolve the symptom. At the end of the 12-week dose adjustment phase, at Visit 4, it will be determined whether meaningful tremor reduction has occurred at the target dose of 300 mg per day or at a lesser but tolerated dose. If not, the participant will discontinue from the study. If benefit has occurred, the subject will be invited to continue taking zonisamide for another 12 weeks, at the conclusion of which the participant will be seen in the final visit (Visit 5). The videotapes will be coded so that the order they were made is not apparent, and the degree of tremor will be rated by a rater who does not know the study participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Essential Tremor
Keywords
essential tremor, zonisamide, clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zonisamide
Arm Type
Experimental
Arm Description
Zonisamide administration and tremor assessment to assess efficacy in reducing essential tremor
Intervention Type
Drug
Intervention Name(s)
Zonisamide
Intervention Description
study drug initially will taken as one 50-mg tablet a day, then the dose increased by one tablet each two weeks, to no more than 3 tablets (150 mg) taken twice a day.
Primary Outcome Measure Information:
Title
The degree of tremor at the end of the dose adjustment phase compared to baseline.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Quality of life.
Time Frame
6 months
Title
Degree of tremor at the end of the extension phase compared to the beginning of the extension phase.
Time Frame
5 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18 or older diagnosis of essential tremor tremor present in both hands for at least one year tremor is bothersome in at least one hand, so that reduction of tremor would improve quality of life able to comply with study visits and procedures has voluntarily signed consent form able to abstain from alcohol for 12 hours prior to each visit, and from caffeine on day prior to visit taking no medications or stable doses of anti-tremor medication for 4 weeks prior to the Baseline visit Exclusion Criteria: medical condition likely to cause hospitalization during the study progressive neurological disorder other than essential tremor history of serious psychiatric illness history of drug or alcohol abuse in past year consumes more than two glasses of wine or equivalent per day has received botulinum toxin injection in past 6 months currently using experimental device has taken experimental drug within 5 half lives of its elimination has received deep brain stimulation in past two weeks or has potential need for this therapy during the study thalamotomy within the past 6 months taking medications judged by investigator to exacerbate tremor has probable cause of tremor other than essential tremor condition likely to interfere with absorption, metabolism or elimination of study drug hepatic disease renal disease history of renal stones history of allergy to sulfonamides
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adrian Handforth, M.D.
Organizational Affiliation
Veterans Affairs Greater Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Greater Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90073
Country
United States

12. IPD Sharing Statement

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A Safety/Efficacy Trial of Zonisamide for Essential Tremor

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