The Effects of Milnacipran on Sleep Disturbance in Fibromyalgia

Completed · Phase 4 · Has a placebo group

Conditions studied: Sleep Disorders, Fibromyalgia, Sleep

In brief

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.

Key facts

Study ID

NCT01234675

Run by

Mansoor Ahmed M.D.

People needed

19

Starts

2010-11-01

Expected to finish

2014-02-01

Last updated by the study team

2019-08-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• Cleveland Sleep Research Center — Middleburg Heights, Ohio, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.