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Efficacy and Safety Study of Topiramate to Treat Restless Legs Syndrome

Primary Purpose

Restless Legs Syndrome

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Topiramate
Sponsored by
Neurocare
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional educational/counseling/training trial for Restless Legs Syndrome focused on measuring Restless Legs Syndrome, Topiramate, Actigraphy, Polysomnography

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: The symptoms of each subject must meet the diagnostic criteria of the International RLS Study Group More than five periodic leg movements per hour recorded during baseline polysomnography (PSG) Each subject must discontinue all treatments for RLS and agreed not to take other RLS treatments during the study Exclusion Criteria: Clinically unstable medical problems History of nephrolithiasis Progressive neurologic disease Inadequate therapeutic response from two previous treatment regimens for RLS Subjects unable to discontinue medications known to cause or suppress RLS Subjects with sleep apnea syndrome Subjects consuming daily more than three beverages containing caffeine

Sites / Locations

  • Neurocare

Outcomes

Primary Outcome Measures

The average number of periodic leg movements during three consecutive nights of actigraphy beginning at the end of the double blind phase

Secondary Outcome Measures

Proportion of time in bed without leg movements during the three consecutive nights of actigraphy beginning at the end of the double blind phase
SF-36 at the last visit of the double blind phase
Score on the RLS Rating Scale (modified) questionnaire at the last visit of the double blind phase
Periodic leg movements during sleep and wakefulness during the PSG recorded at the end of the double blind phase
PSG measures including periodic leg movement arousal index, latency until sustained sleep, sleep efficacy, and wake after sleep onset
Sleep diaries at the last double-blind visit
Epworth sleepiness scale at the last double-blind visit

Full Information

First Posted
September 12, 2005
Last Updated
December 15, 2005
Sponsor
Neurocare
Collaborators
Ortho-McNeil Pharmaceutical
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1. Study Identification

Unique Protocol Identification Number
NCT00200941
Brief Title
Efficacy and Safety Study of Topiramate to Treat Restless Legs Syndrome
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Determine the Effacy and Safety of Topiramate in Subjects With Restless Legs Syndrome (RLS)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
August 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Neurocare
Collaborators
Ortho-McNeil Pharmaceutical

4. Oversight

5. Study Description

Brief Summary
This study is intended to determine whether topiramate is an efficacious and safe treatment for restless legs syndrome.
Detailed Description
Benzodiazepines, levo-dopa/carbidopa, dopamine agonists, anticonvulsants, and opioids have been used with variable success, to treat RLS. Often, RLS patients treated with a benzodiazepine, over the course of several months, develop tolerance to the medication. Also, benzodiazepines can cause confusion or daytime sleepiness and may be addictive. Patients may also develop tolerance to levo-dopa/carbidopa treatment. Because of the short half-life, symptoms may be suppressed for only the first part of the sleep period and then recur later during the night. Rebound has been reported. Worse yet, augmentation, the occurrence of RLS symptoms, often more severe than before treatment began, earlier in the day, may occur in up to 80% of RLS patients treated with levod-dopa/carbidopa. Dopamine agonists, including pergolide, pramipexole, and ropinirole, are effective for some patients but not for others. Common side effects of these drugs include coryza, hypotension, and rash. Of the anticonvulsants, preliminary reports suggest that gabapentin, carbamazepine, and divalproex can suppress RLS symptoms in some patients, especially those with mild RLS. Side effects include sleepiness, ataxia, and weight gain. Opioid treatment for RLS has been described as effective but, aside from the stigma of taking controlled substances regularly, side effects may include nausea, sedation, constipation, and dysequilibrium. Iron supplementation is therapeutic in some patients with iron deficiency and RLS. Preliminary anecdotal data suggest that topiramate reduces RLS symptoms. Topiramate has several potential mechanisms of action including enhancement of GABA-mediated inhibition, which may account for the observed benefit in patients with RLS. Topiramate may be a better alternative than the currently available treatments to suppress RLS symptoms. Like gabapentin, it offers the possibility of decreasing RLS symptoms while also diminishing pain, especially in those patients who have limb pain from neuropathy, radiculopathy, or other causes. Unlike gabapentin, topiramate may help overweight patients with RLS lose weight, if anedotal reports on weight reduction with the medication are correct.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Restless Legs Syndrome
Keywords
Restless Legs Syndrome, Topiramate, Actigraphy, Polysomnography

7. Study Design

Primary Purpose
Educational/Counseling/Training
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
44 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Topiramate
Primary Outcome Measure Information:
Title
The average number of periodic leg movements during three consecutive nights of actigraphy beginning at the end of the double blind phase
Secondary Outcome Measure Information:
Title
Proportion of time in bed without leg movements during the three consecutive nights of actigraphy beginning at the end of the double blind phase
Title
SF-36 at the last visit of the double blind phase
Title
Score on the RLS Rating Scale (modified) questionnaire at the last visit of the double blind phase
Title
Periodic leg movements during sleep and wakefulness during the PSG recorded at the end of the double blind phase
Title
PSG measures including periodic leg movement arousal index, latency until sustained sleep, sleep efficacy, and wake after sleep onset
Title
Sleep diaries at the last double-blind visit
Title
Epworth sleepiness scale at the last double-blind visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The symptoms of each subject must meet the diagnostic criteria of the International RLS Study Group More than five periodic leg movements per hour recorded during baseline polysomnography (PSG) Each subject must discontinue all treatments for RLS and agreed not to take other RLS treatments during the study Exclusion Criteria: Clinically unstable medical problems History of nephrolithiasis Progressive neurologic disease Inadequate therapeutic response from two previous treatment regimens for RLS Subjects unable to discontinue medications known to cause or suppress RLS Subjects with sleep apnea syndrome Subjects consuming daily more than three beverages containing caffeine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael P Biber, MD
Organizational Affiliation
Neurocare
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neurocare
City
Newton
State/Province
Massachusetts
ZIP/Postal Code
02459
Country
United States

12. IPD Sharing Statement

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Efficacy and Safety Study of Topiramate to Treat Restless Legs Syndrome

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