Fatigue, Multiple Sclerosis
Conditions
Brief summary
Multiple sclerosis (MS) is an inflammatory, demyelinating and degenerative disease of the central nervous system and, after trauma, is the most common cause of disability in young adults, affecting more than 400,000 individuals in the US. Of all the symptoms that can occur with MS, chronic fatigue is the most common and disabling, reported by at least 75% of patients at some point. Fatigue limits patients' daily activities, and challenges employment, resulting in substantial socioeconomic consequences. Despite this negative impact, fatigue treatments have been inconsistently studied, in part due to poorly understood underlying pathophysiological mechanisms. Yet to be defined biological processes and lack of clear treatment targets have also hampered the development of drugs for fatigue. As a result, there are no medications approved by the Food and Drug Administration (FDA) for the treatment of MS fatigue. The investigators recently reported that riluzole, a medication with anti-glutamatergic effects, increased the fatigue severity in patients with relapsing MS who had participated in a clinical trial evaluating potential neuroprotective effects of riluzole versus placebo. Three other clinic trials which examined memantine effects on cognition in patient with MS also reported worsening fatigue as a major side effect. Memantine main mechanism of action is blocking the N-methyl D-aspartate (NMDA) glutamate receptor. These observations prompted the investigators that glutamatergic transmission probably plays an important role in fatigue pathogenesis and modulating these pathways could have potential therapeutic effect on MS-related fatigue. A recent paper reported that ketamine, an NMDA receptor blocker with different kinetics compared to memantine, had a strong and prolonged effect in reducing fatigue in bipolar patients who participated in a clinical trial, evaluating anti-depressive effects of ketamine versus placebo. Interestingly, the effect of ketamine on fatigue was independent of its antidepressant effects. The primary objective of this study is to determine if modulating glutamatergic transmission with ketamine is safe and efficacious in improving MS-related fatigue. These objectives will be answered in a proof of concept, randomized controlled trial of ketamine versus an active placebo (midazolam) in patients with relapsing or progressive MS who have clinically significant fatigue. 18 patients with MS and reported fatigue, will be randomized 2:1 to one infusion of ketamine 0.5 mg/kg over 40 minutes versus one infusion of midazolam 0.05 mg/kg over 40 minutes. Midazolam is chosen as an active placebo to keep the participants blinded to participants' medication assignment. Primary outcome of the study will be Daily Fatigue Severity measured daily from day one through day seven post-infusion. Secondary outcomes of the study include other fatigue questionnaires, depression and sleepiness. The length of study will be around 28 days.
Interventions
DRUGKetamine
One intravenous infusion of ketamine 0.5 mg/kg over 40 minutes
DRUGMidazolam
One intravenous infusion of midazolam 0.05 mg/kg over 40 minutes
Sponsors
National Multiple Sclerosis Society
Johns Hopkins University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Age between 18 years 65 years. * Females of childbearing age must have a negative urine pregnancy test at baseline and use an effective method of contraception during the study. * Diagnosis of MS (according to the 2010 McDonald criteria). * Ambulatory (at least 20 feet using bilateral assistance). * Fatigue reportedly present and screening modified fatigue impact scale (MFIS) score \>33. * Internet and email access and able to use a computer or tablet
Exclusion criteria
* Beck Depression Inventory (BDI) score of more than 30. * Neurodegenerative disorders other than relapsing or progressive MS. * Breastfeeding or pregnant. * History of coronary artery disease or congestive heart failure. * Uncontrolled hypertension at screening (history of high blood pressure and screening systolic blood pressure \>160 or diastolic blood pressure\>100). * History of severe liver disease, including cirrhosis. * Terminal medical conditions. * Currently treated for active malignancy. * Alcohol or substance abuse in the past year (except marijuana or other cannabinoids). * A history of intolerance or allergic or anaphylactic reaction to ketamine or midazolam * Clinically unstable medical or psychiatric disorders that require acute treatment as determined by the PI. * History of severe or untreated coronary artery disease or history of congestive heart failure. * History of prior ischemic or hemorrhagic stroke and cerebral vascular aneurysms. * History of recurrent seizures or epilepsy. * Taking any disallowed therapy(ies) as noted in Appendix 2 of the protocol.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Daily Fatigue Severity Score | Baseline (infusion visit) through day 7 | It is a single item question: 'how much fatigue (tiredness, weariness, problems thinking clearly) have you felt today?' with responses from 0 'None at all' to 10 'Extreme Fatigue'. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\]. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Quality of Life in Neurological Disorders (NeuroQol) Fatigue Item Bank Score | Baseline (infusion visit) through day 28 post-infusion | T-score distributions rescale raw scores into standardized scores with a mean of 50 and a standard deviation (SD) of 10. Higher T-scores denote more severe fatigue. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\]. |
| Change in Modified Fatigue Impact Scale (MFIS) Score | Baseline (infusion visit) through Day 28 post-infusion | The total score of the MFIS ranges from 0 to 84. Higher scores denote more severe fatigue. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\]. |
| Change in Epworth Sleepiness Scale Score | Baseline (infusion visit) through day 28 post-infusion | The Epworth Sleepiness Scale score can range from 0 to 24. The higher the score, the higher that person's average sleep propensity in daily life (ASP), or their 'daytime sleepiness'. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\]. |
| Change in Beck Depression Inventory (BDI) Score | Baseline (infusion visit) through day 28 post-infusion | The total score of the BDI ranges from 0 to 63. Higher scores denote more severe depressive symptoms. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\]. |
| Change in Fatigue Severity Scale (FSS) Score | Baseline (infusion visit) through day 28 post-infusion | The total score of the FSS ranges from 9 to 63. Higher scores denote more severe fatigue. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\]. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Ketamine Ketamine: One intravenous infusion of ketamine 0.5 mg/kg over 40 minutes | 12 |
| Midazolam Midazolam: One intravenous infusion of midazolam 0.05 mg/kg over 40 minutes | 6 |
| Total | 18 |
Baseline characteristics
| Characteristic | Midazolam | Total | Ketamine |
|---|---|---|---|
| Age, Continuous | 49 years STANDARD_DEVIATION 8.4 | 45.7 years STANDARD_DEVIATION 11.3 | 44 years STANDARD_DEVIATION 12.4 |
| Race and Ethnicity Not Collected | — | 0 Participants | — |
| Region of Enrollment United States | 6 Participants | 18 Participants | 12 Participants |
| Sex: Female, Male Female | 4 Participants | 11 Participants | 7 Participants |
| Sex: Female, Male Male | 2 Participants | 7 Participants | 5 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 12 | 0 / 6 |
| other Total, other adverse events | 7 / 12 | 0 / 6 |
| serious Total, serious adverse events | 0 / 12 | 0 / 6 |
Outcome results
Primary
Change in Daily Fatigue Severity Score
It is a single item question: 'how much fatigue (tiredness, weariness, problems thinking clearly) have you felt today?' with responses from 0 'None at all' to 10 'Extreme Fatigue'. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\].
Time frame: Baseline (infusion visit) through day 7
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Ketamine | Change in Daily Fatigue Severity Score | -0.05 score on a scale |
| Midazolam | Change in Daily Fatigue Severity Score | -0.05 score on a scale |
Secondary
Change in Beck Depression Inventory (BDI) Score
The total score of the BDI ranges from 0 to 63. Higher scores denote more severe depressive symptoms. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\].
Time frame: Baseline (infusion visit) through day 28 post-infusion
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Ketamine | Change in Beck Depression Inventory (BDI) Score | 0.07 score on a scale |
| Midazolam | Change in Beck Depression Inventory (BDI) Score | 0.07 score on a scale |
Secondary
Change in Epworth Sleepiness Scale Score
The Epworth Sleepiness Scale score can range from 0 to 24. The higher the score, the higher that person's average sleep propensity in daily life (ASP), or their 'daytime sleepiness'. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\].
Time frame: Baseline (infusion visit) through day 28 post-infusion
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Ketamine | Change in Epworth Sleepiness Scale Score | 0.03 score on a scale |
| Midazolam | Change in Epworth Sleepiness Scale Score | 0.11 score on a scale |
Secondary
Change in Fatigue Severity Scale (FSS) Score
The total score of the FSS ranges from 9 to 63. Higher scores denote more severe fatigue. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\].
Time frame: Baseline (infusion visit) through day 28 post-infusion
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Ketamine | Change in Fatigue Severity Scale (FSS) Score | 0.03 score on a scale |
| Midazolam | Change in Fatigue Severity Scale (FSS) Score | 0.22 score on a scale |
Secondary
Change in Modified Fatigue Impact Scale (MFIS) Score
The total score of the MFIS ranges from 0 to 84. Higher scores denote more severe fatigue. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\].
Time frame: Baseline (infusion visit) through Day 28 post-infusion
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Ketamine | Change in Modified Fatigue Impact Scale (MFIS) Score | -0.46 score on a scale |
| Midazolam | Change in Modified Fatigue Impact Scale (MFIS) Score | 0.02 score on a scale |
Secondary
Change in Quality of Life in Neurological Disorders (NeuroQol) Fatigue Item Bank Score
T-score distributions rescale raw scores into standardized scores with a mean of 50 and a standard deviation (SD) of 10. Higher T-scores denote more severe fatigue. Reported score changes are the average point/day score change. The mean score is reported based on this calculation: \[(last day measure - baseline measure) / the number of days in the study\].
Time frame: Baseline (infusion visit) through day 28 post-infusion
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Ketamine | Change in Quality of Life in Neurological Disorders (NeuroQol) Fatigue Item Bank Score | -1.02 score on a scale |
| Midazolam | Change in Quality of Life in Neurological Disorders (NeuroQol) Fatigue Item Bank Score | -0.46 score on a scale |