Cleveland Sleep Research Center
Middleburg Heights, Ohio, 44130, United States
NCT Number: NCT01234675
Fibromyalgia is a condition of chronic widespread pain, sleep disturbance and fatigue. Most of the patients with fibromyalgia complain of either non-restorative sleep or complaints of disturbed sleep due to pain. The study aimed at examining the effects of milnacipran on sleep disturbance in patients with fibromyalgia. The study is a randomized, double-blind, placebo controlled, two way crossover polysomnography (PSG) study to explore the effects of milnacipran on sleep disturbance. Patients received either milnacipran 50 mg twice a day (BID) or matching placebo.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Middleburg Heights, Ohio, 44130, United States
The sleep disturbance in fibromyalgia is characterized as non-restorative in nature, and is defined as a feeling of light sleep, independent of duration, and as non-refreshing. As such, these patients wake up in the morning and complain of stiffness and overall aching of the body.
It is well known that reciprocal relationship exists between sleep and pain, with sleep disturbances being an important contributor to morbidity in fibromyalgia. Milnacipran, a selective serotonin norepinephrine receptor inhibitor (SNRI), was approved by the Food and Drug Administration (FDA) for the management of fibromyalgia. Although milnacipran has extensively been studied in fibromyalgia patients, but there is no objective measure, i.e., the use of overnight polysomnography, to determine its effects on sleep.
The study was undertaken to evaluate the effects of milnacipran on PSG determined measures of sleep in patients with fibromyalgia. The study also evaluated the impact of milnacipran on subjective measures of sleep and fibromyalgia symptoms.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Liver disease, blood disorder, autoimmune disease, endocrine, cardiovascular, hypertension, renal, hepatic, gastrointestinal, or neurological disorder, active peptic ulcer or inflammatory bowel disease
50 mg twice daily
Other names: Savella
50 mg twice daily
Other names: Sugar pill
Time frame: 4-Week maintenance treatment with milnacipran and placebo
Number of awakenings after defined sleep onset until lights on.
Time frame: 4-Week maintenance treatment with milnacipran and placebo
Percentage of time spent asleep while in bed
Time frame: 4-Week maintenance treatment with milnacipran and placebo
Wake time after defined sleep onset until lights on.
Time frame: 4-Week treatment with milnacipran and placebo
It is defined as time from lights out to the first consecutive 2 minutes of uninterrupted sleep.
Time frame: 4-Week treatment with milnacipran and placebo
Total sleep of all Rapid Eye Movement (REM) and Non- Rapid Eye Movement Sleep (NTREM) from lights out to lights on.
Time frame: 4-Week treatment with milnacipran and placebo
Number of arousals per hour of sleep
Time frame: 4-Week treatment with milnacipran and placebo
Time spent in stage 3 of non-rapid eye movement sleep and often referred to as deep sleep.
Time frame: 4-Week treatment with milnacipran and placebo
This is a subjective index derived from the medical outcomes study sleep scale (MOS-SS) scored on a 0-100 possible range with higher scores indicating more severe sleep disruption. The scale is a self-report instrument consisting of 12 items that assess perceived initiation and maintenance of sleep, respiratory problems during sleep, sleep duration, perceived adequacy of sleep and daytime somnolence.
Time frame: 4-Week treatment with milnacipran and placebo
Sleep quality measure derived from daily sleep diary rating ranging from 0 ("very poor") to 10 ("excellent")
Time frame: 4-Week treatment with milnacipran and placebo
The scale is a 9-item self-report of fatigue in the past week and scored on a 7-point scale with 1 = strongly disagree and 7 = strongly agree. Scores range from 9 to 63 with higher scores indicating higher fatigue severity. A total score greater or equal to 36 suggests fatigue.
Time frame: 4-Week treatment with milnacipran and placebo
The scale is composed of 10 items relating to fibromyalgia symptoms experienced in the past week. Score ranges from 0 to 100 with higher scores indicating a greater effect of fibromyalgia on a person's life.
Time frame: 4-Week treatment with milnacipran and placebo
The score is derived from the BPI scale and measures pain intensity in the past 24 hour. The pain severity score is derived as the average score of 4 pain items assessing pain at its "worst", "least", "average" and "now" and ranges from 0-10 with higher scores reflecting greater pain
Time frame: 4-Week treatment with milnacipran and placebo
The score is derived from the BPI scale and measures the effect of pain on functioning in the past 24 hour. It is the average score of 7 items interfering with general activity, mood, walking ability, normal work, relations with other people, sleep and enjoyment of life. Score ranges from 0-10 with higher scores reflecting greater interference.
Mansoor Ahmed M.D.
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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