Phase
Condition
Sleep Apnea Syndromes
Sleep Disorders
Multiple Sclerosis
Treatment
N/AClinical Study ID
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
18-65 years old
Diagnosis of clinical MS as defined by the 2010 McDonald criteria
Have either relapsing remitting, primary progressive or secondary progressive forms ofMS
expanded disability status scale ≤5
Complaint of fatigue defined subjective lack of physical and/or mental energy that isperceived by the individual or caregiver to interfere with the usual and desiredactivity.
Berlin questionnaire score of ≥2 35
Mild to moderate OSA defined as Apnea hypopnea index (AHI) of ≥ 5 and < 30 events/houron baseline ambulatory PSG
Exclusion
Exclusion Criteria:
Prior diagnosis, past or current treatment for sleep related breathing disorder
Severe sleep apnea defined as AHI ≥ 30 events/hour on baseline ambulatory PSG,
Prior diagnosis of restless leg syndrome, parasomnias, insomnia, and narcolepsy
Prior diagnosis of pulmonary disease: asthma, chronic obstructive pulmonary diseaseand bronchiectasis
Diagnosis of clinical depression or Center for epidemiologic studies-depressionscale(CES-D)score of ≥ 16 36,37
An acute MS exacerbation in the last 3 months. If patient has an acute exacerbationduring the study, the patient will be excluded from the study as this can be a causefatigue
Started on any disease modifying treatment (either primary or second line agents) orhave switched to a second therapy in the last 6 month poor sleep and fatigue can beside effects.
Current use of sedative-hypnotics medications, tricyclic, antidepressants, ortrazodone.
Started or change in dose within the last 3 months of amantadine, modafinil,armodafinil, or other stimulating agent for MS related fatigue
Pregnancy
Unstable medical or psychiatric condition
Study Design
Study Description
Connect with a study center
Northwestern UNiversity, Department of Neurology
Chicago, Illinois 60611
United StatesSite Not Available

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