Fatigue, Multiple Sclerosis
Conditions
Brief summary
The purpose of this study is to determine whether aspirin is effective for treatment of fatigue caused by multiple sclerosis (MS).
Detailed description
Fatigue is the most common symptom of multiple sclerosis (MS), affecting up to 90% of people with the disease. MS-related fatigue can be disabling even when other features of MS are mild. It can interfere with physical activity, memory and thinking, social and family activities, and ability to work. Initial treatment consists of energy conservation techniques such as rest periods or naps but when these approaches fail doctors usually recommend a trial of medications. Amantadine, modafinil, and other stimulants are commonly used but help only about half of those who try them. It is unlikely that these drugs directly affect the cause of MS-related fatigue. It has been difficult to develop new drug therapies for MS-related fatigue because we do not fully understand its causes and do not have precise ways to measure it. We rely on a person's self-report about their fatigue but individuals experience and report fatigue differently. Recent research has shown that some fatigue aspects, such as difficulty maintaining mental concentration (cognitive fatigue) and physical activity (motor fatigue), can be measured more precisely and require further study. We recently reported results from a study showing that people taking the equivalent of four regular aspirin tablets (1300 mg) daily had reduced MS-related fatigue compared with placebo (sugar pill). The current proposal will attempt to confirm the benefit of aspirin in a larger group of people and to determine if the benefit is related to inflammation. One hundred and thirty-five people with MS-related fatigue will participate at MS clinics at three Mayo Clinic sites. Participants will complete questionnaires that ask about the severity and impact of their fatigue, memory testing to assess cognitive fatigue, and have blood testing to measure markers of inflammation. At the Arizona site, participants will also do strength testing in a motor laboratory to assess motor fatigue. After obtaining two separate baseline evaluations, the participants will be randomly assigned treatment such that one-third will receive 1300 mg per day of aspirin, one-third will receive 162 mg per day of aspirin and one-third will receive a matching placebo. All participants will then return to the clinic on two more occasions over the next eight weeks to repeat the questionnaires, memory and strength testing, blood tests, and report any side-effects. At the end of the study, the results of one of the fatigue questionnaires will be analyzed to determine if aspirin significantly improved fatigue compared with the placebo. The results of other questionnaires and the memory and strength testing will be analyzed as supportive evidence. If this study is successful, it will provide strong scientific evidence that aspirin helps MS-related fatigue. It will add an important new option for treatment of all MS patients that is also familiar, inexpensive, and has a good long-term safety record. At the same time, it will allow us to better understand the causes of MS-related fatigue and how to measure it more precisely. This information will be extremely useful for development of other therapies in the future.
Interventions
DRUGHigh Dose Aspirin (1300 mg/day)
1300 milligrams per day (the equivalent of 4 regular aspirin tablets) taken by mouth as two tablets, twice a day in the morning and at noon for 8 weeks
DRUGLow Dose Aspirin (162 mg/day)
162 milligrams per day (the equivalent of 2 baby aspirin tablets) taken by mouth as two tablets, twice a day in the morning and at noon for 8 weeks
DRUGPlacebo
Placebo tablets matching the active aspirin tablets in appearance, taken as two tablets, twice per day for 8 weeks
Sponsors
National Multiple Sclerosis Society
Mayo Clinic
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
* Confirmed relapsing-remitting or secondary progressive multiple sclerosis, * Ambulatory for distance of at least 100 meters without gait assistance, * Persistent fatigue for at least 8 weeks that is not attributable to causes other than MS, and * Will be able to complete questionnaires and cognitive testing.
Exclusion criteria
1. Other evident causes for fatigue: * Untreated depression or screening Center for Epidemiologic Studies Depression (CES-D) scale greater than 28 * Significant cognitive impairment (Baseline Short Test of Mental Status score of less than 29/38) * Narcolepsy, uncontrolled sleep apnea, or other primary sleep disorder judged to be likely a major contributor to fatigue * Screening Epsworth Sleepiness Scale score greater than 15 * Uncontrolled hypothyroidism or anemia * Other medical illness judged by the investigator to affect the participant's fatigue complaints including current viral, bacterial, mycobacterial, or fungal infection 2. MS Disease Activity and Treatment: * Clinical exacerbations within 2 weeks prior to screening visit * Corticosteroid use within 4 weeks prior to screening visit * Beta-interferon, glatiramer acetate, immunosuppressant drugs (mitoxantrone, azathioprine, etc.) are permitted if a stable dose has been used for greater than or equal to 4 weeks and there is no temporal association of drug administration with perceived fatigue; elective on-study dose/regimen changes are not permitted 3. Current or Recent Fatigue Therapy and Other Medications: * Use of more than two doses of ASA (aspirin) greater than 81 mg/d within 2 weeks of screening visit * Use of MS fatigue medications within 2 weeks of screening visit (including amantadine or Central Nervous System stimulants such as modafinil, methylphenidate, and pemoline) * Symptomatic medications (antidepressants, anti-spasticity agents, non-narcotic analgesics) are permitted if a stable dose has been used for \>4 weeks prior to screening for antidepressants and \>2 weeks prior to screening for other symptomatic therapies and there is no temporal association of drug administration with perceived fatigue; elective on-study dose changes are not permitted. * Current use of acetazolamide, antiplatelet agents or anticoagulants, COX-2 inhibitors, methotrexate, oral hypoglycemic medications 4. Medical Contraindications to ASA use: * Allergy to ASA or Non-Steroidal Anti-Inflammatory drugs * Syndrome of asthma, rhinitis and nasal polyps * History of confirmed peptic ulcer or gastrointestinal or severe gynecological bleeding 5. General Health Concerns: * Significant uncontrolled disease of cardiovascular, pulmonary, hepatic, renal, endocrine, rheumatological, neurological, gynecological, or gastrointestinal systems * Pregnancy or unwillingness to utilize contraception * History of alcohol or drug abuse within 6 months of screening or current alcohol intake \>3 drinks/day 6. Laboratory Exclusions (available values obtained within 8 weeks prior to screening visit are acceptable for all except the pregnancy test) * Positive pregnancy test * Hemoglobin less than 11.0 g/dL (women) or 13.0 g/dL (men) * Platelet count \< 120, 000/μL * Serum creatinine level \> 1.4 mg/dL (women) or 1.6 mg/dL (men) * Aspartate aminotransferase (AST/SGOT) or alanine aminotransferase (ALT/SGPT) level greater than 2.5 times the upper limit of normal
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Modified Fatigue Impact Scale Score | Baseline, 8 weeks | The Modified Fatigue Impact Scale is a list of 21 statements describing how fatigue may affect a person's functioning. Answers ranging from 0 (Never) to 4 (Almost always) were provided by the study subjects for the prior 4 week period. A total score was tallied from a possible 0 (no fatigue impact) to 84 (almost always impacted by fatigue). A lower total score indicates less fatigue-related impact while a higher total score indicates greater fatigue-related impact on a subject's functioning. |
Countries
United States
Participant flow
Recruitment details
Participants with Multiple Sclerosis were recruited from three Mayo Clinic sites (Arizona, Minnesota and Florida) beginning in July, 2007.
Participants by arm
| Arm | Count |
|---|---|
| High Dose Aspirin High Dose Aspirin; 1300 milligrams of aspirin per day, taken by mouth as two tablets, twice per day for 8 weeks | 21 |
| Low Dose Aspirin Low Dose Aspirin; 162 milligrams of aspirin per day taken by mouth as two tablets, twice per day for 8 weeks | 20 |
| Placebo Placebo tablets, matching the active aspirin tablets in appearance, taken by mouth twice per day for 8 weeks | 21 |
| Total | 62 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | Withdrawal by Subject | 4 | 5 | 1 |
Baseline characteristics
| Characteristic | High Dose Aspirin | Low Dose Aspirin | Placebo | Total |
|---|---|---|---|---|
| Age, Continuous | 46.6 years STANDARD_DEVIATION 8.6 | 47.0 years STANDARD_DEVIATION 10.3 | 47.4 years STANDARD_DEVIATION 8 | 47.0 years STANDARD_DEVIATION 9 |
| Region of Enrollment United States | 21 participants | 20 participants | 21 participants | 62 participants |
| Sex: Female, Male Female | 17 Participants | 15 Participants | 18 Participants | 50 Participants |
| Sex: Female, Male Male | 4 Participants | 5 Participants | 3 Participants | 12 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — |
| other Total, other adverse events | 5 / 17 | 0 / 15 | 3 / 20 |
| serious Total, serious adverse events | 0 / 17 | 0 / 15 | 0 / 20 |
Outcome results
Primary
Modified Fatigue Impact Scale Score
The Modified Fatigue Impact Scale is a list of 21 statements describing how fatigue may affect a person's functioning. Answers ranging from 0 (Never) to 4 (Almost always) were provided by the study subjects for the prior 4 week period. A total score was tallied from a possible 0 (no fatigue impact) to 84 (almost always impacted by fatigue). A lower total score indicates less fatigue-related impact while a higher total score indicates greater fatigue-related impact on a subject's functioning.
Time frame: Baseline, 8 weeks
Population: 62 patients were randomized; of these, 6 did not receive the intervention and an additional 4 discontinued without providing followup data. Therefore 52 were included in the analysis. The Wk 4 MFIS score was used if the subject withdrew prior to Wk 8. 1 subject each in the High Dose and Placebo groups provided MFIS data at Wk 4 but not Wk 8.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| High Dose Aspirin | Modified Fatigue Impact Scale Score | MFIS Total Score at Baseline | 48 units on a scale | Standard Deviation 13 |
| High Dose Aspirin | Modified Fatigue Impact Scale Score | Change in MFIS Total Score | -11.4 units on a scale | Standard Deviation 13.9 |
| High Dose Aspirin | Modified Fatigue Impact Scale Score | MFIS Total Score at 8 Weeks | 37 units on a scale | Standard Deviation 11 |
| Low Dose Aspirin | Modified Fatigue Impact Scale Score | MFIS Total Score at 8 Weeks | 45 units on a scale | Standard Deviation 17 |
| Low Dose Aspirin | Modified Fatigue Impact Scale Score | MFIS Total Score at Baseline | 50 units on a scale | Standard Deviation 15 |
| Low Dose Aspirin | Modified Fatigue Impact Scale Score | Change in MFIS Total Score | -5.1 units on a scale | Standard Deviation 15.7 |
| Placebo | Modified Fatigue Impact Scale Score | Change in MFIS Total Score | -5.5 units on a scale | Standard Deviation 9.8 |
| Placebo | Modified Fatigue Impact Scale Score | MFIS Total Score at Baseline | 49 units on a scale | Standard Deviation 13 |
| Placebo | Modified Fatigue Impact Scale Score | MFIS Total Score at 8 Weeks | 44 units on a scale | Standard Deviation 13 |