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Mexiletine for the Treatment of Muscle Cramps in ALS

Mexiletine for the Treatment of Muscle Cramps in ALS

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01811355
Enrollment
23
Registered
2013-03-14
Start date
2013-05-31
Completion date
2016-05-31
Last updated
2017-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Cramps in Amyotrophic Lateral Sclerosis

Keywords

Muscle cramps, Cramp, ALS, Amyotrophic Lateral Sclerosis, Lou Gehrig's disease, Motor Neuron Disease, MND

Brief summary

The purpose of this study is to determine if mexiletine is effective for the treatment of muscle cramps in Amyotrophic Lateral Sclerosis (ALS).

Detailed description

Background: Many ALS patients suffer from painful muscle cramps, but unfortunately we do not have any medication proven to help muscle cramps in ALS. Reducing the pain caused by cramps - which can be debilitating - could help people living with ALS. Muscle cramps are sudden, painful, and involuntary contractions of a muscle. They are caused by nerve dysfunction. When we examine nerves and muscles electrically, we see cramps as bursts of high-frequency (up to150 Hz) firing of the motor nerve cells. Cramps in ALS are believed to be the result of an increase of persistent sodium currents in the sick lower motor nerve cells. A medication called Quinine was for many years the commonly used drug for controlling cramps in ALS, but the FDA has advised against its use for cramps because of its potential risks (e.g., death). Today there is no agreement on how to treat cramps in the ALS. The American Academy of Neurology recently encouraged further studies of the treatment of muscle cramps and suggested lidocaine as one of a few drugs of special interest. Mexiletine: Mexiletine is a medication closely related to lidocaine that can be taken by mouth (instead of being injected). Mexiletine stops the type of sodium currents that are thought to cause muscle cramps. Mexiletine is a relatively older medication that has been extensively studied in humans. It has been shown to reduce the electrical measures of muscle cramps for other disease conditions. For example, in patients with another severe nerve disease - Machado-Joseph disease (SCA3) - mexiletine treatment led to a decrease in the average number of muscle cramps from 24 to 3 cramps per month.. The safety profile of mexiletine is good, with the most frequent side effects being nausea or other abdominal symptoms. These side effects are rare at the doses (300 mg/day) used in this study. In patients with normal heart function, mexiletine has a minimal effect on heart rhythm. In previous clinical trials, no subject developed any serious heart rate problem. Experimental Plan: Using multiple sites within the State of California we will quickly enroll a small number (N=30) of ALS patients with severe muscle cramps. The study is a double-blinded, placebo controlled (i.e., the investigator and the participant does not know if the pills contain mexiletine or placebo), crossover (all subjects receive two weeks of mexiletine and two weeks of placebo) study. After a one week run in, participants will be evaluated on their ability to fill out the cramp diary. Participants who filled out their diary will be randomly assigned to either mexiletine or placebo for their first two weeks. For the first three days of each 2-week period, one 150mg capsule will be taken at bed time. For day 4 to 14 one capsule twice per day will be taken. Each treatment period will be 2 weeks with an intervening 1 week washout period - for a total study length of 6 weeks. Safety will be monitored with liver function studies and EKG's.

Interventions

DRUGMexiletine

Sodium channel blocker

DRUGPlacebo

Placebo

Sponsors

University of California, Davis
CollaboratorOTHER
ALS Association
CollaboratorOTHER
Bjorn Oskarsson, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* ALS diagnosed according to El Escorial criteria (Awaji version) as: Possible, Probable, or Definite. * Experiencing cramps as a moderate or severe symptom as defined by willingness to take a medication for the symptom * ≥2 cramps per week during run in week * Life expectancy \> 6 months, estimated by clinician * Able to take drug capsule by mouth * No significant EKG abnormality on screening * aspartate aminotransferase / alanine aminotransferase \<2x upper limit of normal measured at screening * Having successfully filled out the cramp diary and cramp and fasciculation scales on six out of the last seven days of run in period

Exclusion criteria

* Inability to communicate by telephone or email * Allergy/ known sensitivity to mexiletine * Prior use of mexiletine * AV block unless subject has pacemaker * Cardiac arrhythmia * Prior myocardial infarction * Other significant EKG abnormality * Liver disease * History of leucopenia (WBC \<3,500/mm3) * Epilepsy * Other serious and unstable medical condition * Pregnant woman * Breastfeeding woman * Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements * Use of quinidine (alone or as a component of Nuedexta®) during the study * Inability or unwillingness of subject to give written informed consent * Woman of childbearing potential, not willing to use at least two approved methods of contraception * Use of a prohibited medication during study

Design outcomes

Primary

MeasureTime frameDescription
Daily Muscle Cramps6 weeksThe average of the daily recording of number of muscle cramps that occurred in the last 24 hours- over a 6 week period.
Cramp Severity6 weeksDaily cramp severity was rated on the 100-unit visual analog scale. Scores ranged from 0 to 100, with 100 being the greatest amount of cramp severity

Countries

United States

Participant flow

Pre-assignment details

Of 28 patients who signed consent, 5 did not meet inclusion criteria because of past myocardial infarction (n=1), long QT syndrome (n=1), AV block (n=1), no muscle cramps (n=1), and hospitalization during the screening period that resulted in inability to complete a screening diary and follow-up (n=1) .

Participants by arm

ArmCount
Total Subjects Enrolled
A total of 23 subjects were enrolled. 11 were randomized to receive study drug first, followed by placebo. 12 subjects received placebo first and study drug second. Overall participant characteristics are displayed in the baseline table.
23
Total23

Baseline characteristics

CharacteristicTotal Subjects Enrolled
Age, Customized
Years
62.4 years
STANDARD_DEVIATION 12.5
Ethnicity (NIH/OMB)
Hispanic or Latino
3 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
20 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
1 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
22 Participants
Region of Enrollment
United States
23 participants
Sex/Gender, Customized
females
8 Participants
Sex/Gender, Customized
males
15 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 230 / 21
other
Total, other adverse events
9 / 233 / 21
serious
Total, serious adverse events
0 / 230 / 21

Outcome results

Primary

Cramp Severity

Daily cramp severity was rated on the 100-unit visual analog scale. Scores ranged from 0 to 100, with 100 being the greatest amount of cramp severity

Time frame: 6 weeks

Population: Among the 21 patients who completed the study, 1 patient did not return the outcome diary, which resulted in 20 patients available for analysis.

ArmMeasureGroupValue (MEAN)Dispersion
Mexiletine First/Placebo SecondCramp SeverityPlacebo Dose43.6 units on a scaleStandard Deviation 31
Mexiletine First/Placebo SecondCramp SeverityMexiletine Dose23.1 units on a scaleStandard Deviation 16.8
Mexiletine First/Placebo SecondCramp SeverityDifference Between20.5 units on a scaleStandard Deviation 40.6
Placebo First/Mexiletine SecondCramp SeverityPlacebo Dose44.7 units on a scaleStandard Deviation 26.7
Placebo First/Mexiletine SecondCramp SeverityMexiletine Dose32.8 units on a scaleStandard Deviation 27.7
Placebo First/Mexiletine SecondCramp SeverityDifference Between12.0 units on a scaleStandard Deviation 18.1
Primary

Daily Muscle Cramps

The average of the daily recording of number of muscle cramps that occurred in the last 24 hours- over a 6 week period.

Time frame: 6 weeks

Population: Among the 21 patients who completed the study, 1 patient did not return the outcome diary, which resulted in 20 patients available for analysis.

ArmMeasureGroupValue (MEAN)Dispersion
Mexiletine First/Placebo SecondDaily Muscle CrampsPlacebo Dose6.1 Cramps per 24 hoursStandard Deviation 8.1
Mexiletine First/Placebo SecondDaily Muscle CrampsMexiletine Dose4.9 Cramps per 24 hoursStandard Deviation 8
Mexiletine First/Placebo SecondDaily Muscle CrampsDifference Between1.2 Cramps per 24 hoursStandard Deviation 2.9
Placebo First/Mexiletine SecondDaily Muscle CrampsPlacebo Dose4.7 Cramps per 24 hoursStandard Deviation 4.2
Placebo First/Mexiletine SecondDaily Muscle CrampsMexiletine Dose2.5 Cramps per 24 hoursStandard Deviation 2.8
Placebo First/Mexiletine SecondDaily Muscle CrampsDifference Between2.2 Cramps per 24 hoursStandard Deviation 2.2

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026