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Aspirin for Treatment of Multiple Sclerosis-Related Fatigue
This study is currently recruiting participants.
Verified by Mayo Clinic, April 2007
Sponsors and Collaborators: Mayo Clinic
National Multiple Sclerosis Society
Information provided by: Mayo Clinic
ClinicalTrials.gov Identifier: NCT00467584
  Purpose

The purpose of this study is to determine whether aspirin is effective for treatment of fatigue caused by multiple sclerosis (MS).


Condition Intervention Phase
Multiple Sclerosis
Drug: Aspirin
Phase III

MedlinePlus related topics: Multiple Sclerosis
Drug Information available for: Acetylsalicylic acid
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Aspirin for Treatment of Multiple Sclerosis-Related Fatigue

Further study details as provided by Mayo Clinic:

Primary Outcome Measures:
  • Modified Fatigue Impact Scale score at 8 weeks [ Time Frame: 8 weeks ]

Secondary Outcome Measures:
  • Visual Analog Scale score at 8 weeks [ Time Frame: 8 weeks ]
  • Cognitive fatigue measure at 8 weeks [ Time Frame: 8 weeks ]
  • Motor fatigue measure at 8 weeks [ Time Frame: 8 weeks ]

Estimated Enrollment: 135
Study Start Date: March 2007
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.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • Confirmed relapsing-remitting or secondary progressive multiple sclerosis,
  • Ambulatory for distance of at least 100 m 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:

  • Other evident causes for fatigue,
  • Recent MS disease activity or specific changes in MS therapy,
  • Current use of ASA or other NSAIDs,
  • Use of CNS stimulants,
  • Use of medications that contraindicate the use of ASA, ASA allergy or sensitivity,
  • History of peptic ulcer disease or GI bleed,
  • Alcohol abuse,
  • Pregnancy, and
  • Laboratory abnormalities.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00467584

Locations
United States, Arizona
Mayo Clinic Recruiting
Scottsdale, Arizona, United States, 85259
Contact: Teri Radam     480-301-8756     radam.teresa@mayo.edu    
Principal Investigator: Dean M. Wingerchuk, M.D., MSc            
Sponsors and Collaborators
Mayo Clinic
National Multiple Sclerosis Society
Investigators
Principal Investigator: Dean M. Wingerchuk, M.D., MSc Mayo Clinic
  More Information

Study ID Numbers: 06-004850
Study First Received: April 26, 2007
Last Updated: April 27, 2007
ClinicalTrials.gov Identifier: NCT00467584  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Autoimmune Diseases
Fatigue
Multiple Sclerosis
Aspirin
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Demyelinating diseases
Sclerosis
Autoimmune Diseases of the Nervous System

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Molecular Mechanisms of Pharmacological Action
Immune System Diseases
Cyclooxygenase Inhibitors
Hematologic Agents
Nervous System Diseases
Physiological Effects of Drugs
Enzyme Inhibitors
Fibrinolytic Agents
Cardiovascular Agents
Pharmacologic Actions
Fibrin Modulating Agents
Pathologic Processes
Analgesics, Non-Narcotic
Sensory System Agents
Therapeutic Uses
Platelet Aggregation Inhibitors
Anti-Inflammatory Agents, Non-Steroidal
Analgesics
Peripheral Nervous System Agents
Antirheumatic Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on January 15, 2009