Hypnotics to Improve Polysomnography Yield: Eszopiclone vs Ramelteon?
Information source: Southern California Institute for Research and Education
Information obtained from ClinicalTrials.gov on October 19, 2009 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Obstructive Sleep Apnea
Intervention: Rozerem (Ramelteon) (Drug); Lunesta (Eszopiclone) (Drug); Placebo (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: Southern California Institute for Research and Education Official(s) and/or principal investigator(s): Catherine S. Sassoon, MD, Principal Investigator, Affiliation: VA Long Beach Healthcare System
Overall contact: Catherine S. Sassoon, MD, Phone: (562) 826-5839, Email: catherine.sassoon@va.gov
Summary
This study is being conducted to determine if eszopiclone is as effective as ramelteon when
used as a pre-medication (sleeping pill) in sleep studies performed to diagnose and treat
sleep apnea.
Clinical Details
Official title: Hypnotics to Improve Polysomnography Yield: Eszopiclone vs Ramelteon?
Study design: Diagnostic, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: Non-usable and poor quality PSGs and CPAP intolerance
Detailed description:
Many Veterans suffer from sleep disordered breathing with a high prevalence of undiagnosed
obstructive sleep apnea. One test that can be effective in the diagnosis of sleep apnea is
the polysomnogram (PSG). Split-night PSG consists of a diagnostic phase in the first half
of the night and a continuous positive airway pressure titration (CPAP) in the second half
of the night. CPAP is the standard, most effective therapy for obstructive sleep apnea.
Due to the unfamiliar sleep environment of the laboratory and instrumentation that must be
used (application of electroencephalogram leads), patients are frequently not able to sleep
adequately. In these cases, the PSG must be repeated. Oral hypnotic agents are often used
as a pre-medication to increase the yield of PSG in an attempt to decrease the need for
repeat studies.
Numerous data is available on the effects of premedication with oral short-acting hypnotics
on PSG quality and efficacy of CPAP titration. In one study, eszopiclone, a
nonbenzodiazepine gaba-receptor agonist short-acting hypnotic, has been shown to improve PSG
quality and CPAP titration. Another short-acting hypnotic, ramelteon, was recently approved
by FDA but the effects of ramelteon in improving PSG quality and efficacy of CPAP titration
are unclear. The advantage of ramelteon over eszopiclone is the lack of drug dependency or
abuse potential. This study aims to evaluate the efficacy of ramelteon compared to
eszopiclone when administered prior to split-night PSG and CPAP titration.
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Referred by VA Long Beach Sleep Clinic at their initial evaluation during outpatient
consultation for suspect obstructive sleep apnea.
Exclusion Criteria:
- Sleep disorders other than obstructive sleep apnea
- No prior PSG
- Uncontrolled medical condition
- Prior known adverse reaction to eszopiclone or ramelteon
- Liver disfunction
- Current alcohol abuser
- Current illicit drug abuser
- Alcohol consumption 12 hours prior to polysomnography
- Decompensated psychiatric disorders
- Severe dementia
- Concomitant use of benzodiazepines, trazodone, narcotics, barbiturates or other
medications with sedative or hypnotic effects
Locations and Contacts
Catherine S. Sassoon, MD, Phone: (562) 826-5839, Email: catherine.sassoon@va.gov
VA Long Beach Healthcare System, Long Beach, California 90822-5201, United States; Recruiting Catherine S. Sassoon, MD, Principal Investigator Sterling Malish, MD, Sub-Investigator
Additional Information
Southern California Institute for Research and Education Website
Related publications: Lettieri CJ, Quast TN, Eliasson AH, Andrada T. Eszopiclone improves overnight polysomnography and continuous positive airway pressure titration: a prospective, randomized, placebo-controlled trial. Sleep. 2008 Sep 1;31(9):1310-6.
Starting date: December 2008
Ending date: December 2009
Last updated: August 3, 2009
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