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Completed

NCT Number: NCT01234675

The Effects of Milnacipran on Sleep Disturbance in Fibromyalgia

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Cleveland Sleep Research Center

Middleburg Heights, Ohio, 44130, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men or women at least 18 years or older
  • Diagnosis of fibromyalgia
  • Clinically significant sleep disturbance, defined as difficulty in maintaining sleep (wake after sleep onset and arousal index) at least three times per week for at least one month
  • Understand and willing to cooperate with the study procedures
  • Maintain a normal sleep schedule, with daytime-awake and nighttime-sleep schedule, with customary bedtime between 9 PM and midnight, and rise time 5 AM and 9 AM
  • Patients who are able to speak, read, and understand English language and able to follow the study protocol, and are able to sign the informed consent

Exclusion criteria

  • Subject has any of the following medical conditions:

Liver disease, blood disorder, autoimmune disease, endocrine, cardiovascular, hypertension, renal, hepatic, gastrointestinal, or neurological disorder, active peptic ulcer or inflammatory bowel disease

  • Significant sleep apnea
  • Periodic leg movement disorder (PLMD) or restless legs syndrome (RLS)
  • Any form of severe psychiatric illness, moderate to severe depression, including significant risk of suicide
  • Patients with uncontrolled glaucoma
  • Inability to discontinue the prohibited medications
  • Female of childbearing potential not using birth control measures; or lactating.
  • History of alcohol, narcotic, benzodiazepines or other substance abuse within the past one year.
  • Patient on prohibited medication will include but not limited to:
  • Anxiolytics, anti-convulsants, antipsychotics, lithium, barbiturates, anti-histamines, monoamine oxidase inhibitors, or medications that affect sleep
  • Any prescription or over the counter stimulants
  • Medications that are contraindicated with the use of milnacipran
  • Excessive caffeine use, defined as a consumption of more than 500 mg of caffeine or other xanthines, smoking >1/2 a pack/day or alcohol use >14 units/week
  • History of allergy to milnacipran.

Treatment and study plan

Milnacipran

Drug

50 mg twice daily

Other names: Savella

Placebo

Drug

50 mg twice daily

Other names: Sugar pill

Primary outcomes

  1. Number of Awakenings After Sleep Onset (NAASO)

    Time frame: 4-Week maintenance treatment with milnacipran and placebo

    Number of awakenings after defined sleep onset until lights on.

  2. Sleep Efficiency (SE)

    Time frame: 4-Week maintenance treatment with milnacipran and placebo

    Percentage of time spent asleep while in bed

  3. Wake After Sleep Onset (WASO)

    Time frame: 4-Week maintenance treatment with milnacipran and placebo

    Wake time after defined sleep onset until lights on.

Secondary outcomes

  1. Latency to Persistent Sleep Onset (LPS)

    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.

  2. Total Sleep Time (TST)

    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.

  3. Arousal Index (AI)

    Time frame: 4-Week treatment with milnacipran and placebo

    Number of arousals per hour of sleep

  4. Slow Wave Sleep (SWS)

    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.

  5. Sleep Problem Index 2, Medical Outcomes Study Sleep Scale (MOS-SS)

    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.

  6. Sleep Quality Scale

    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")

  7. Fatigue Severity Scale (FSS) Total Score

    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.

  8. Fibromyalgia Impact Questionnaire (FIQ) Total Score

    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.

  9. Brief Pain Inventory (BPI) Mean Severity Score

    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

  10. Brief Pain Inventory (BPI) Mean Interference Score

    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.

Sponsors and collaborators

Lead sponsor

Mansoor Ahmed M.D.

Other

Collaborators

  • Forest Laboratories

Registry information

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Nov 4, 2010
Registry last updated
Aug 21, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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