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Phase 2 N=23 Randomized Quadruple-blind Treatment

Clarithromycin for the Treatment of Hypersomnia

Hypersomnia · Idiopathic Hypersomnia · Narcolepsy

Enrolled (actual)
23
Serious AEs
0.0%
Results posted
Jun 2014
Primary outcome: Primary: Psychomotor Vigilance Task (PVT) Reaction Time — 279.1; 311.6; 333.8 Msec — p=0.47

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Clarithromycin followed by placebo (Drug); Placebo then Clarithromycin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Lynn Marie Trotti
Primary completion
Sep 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Psychomotor Vigilance Task (PVT) Reaction Time
279.1; 311.6; 333.8 0.47
SECONDARY
PVT Median Reaction Time at Week 1
285.4; 308.4; 333.8 0.63
SECONDARY
PVT Number of Lapses
5.7; 10.3; 6.5 0.64
SECONDARY
Epworth Sleepiness Scale
10.1; 14.1; 15.0 0.002 sig
SECONDARY
FOSQ
16.6; 14.4; 13.9 0.002 sig
SECONDARY
SF-36, Vitality Subscale
48.9; 28.0; 25.0 0.01 sig
SECONDARY
PSQI
5.8; 6.3; 6.7 0.76

Summary

The term 'hypersomnia' describes a group of symptoms that includes severe daytime sleepiness and sleeping long periods of time (more than 10 hours per night). Sometimes, hypersomnia is caused by a problem with the quality of sleep occurring at night, for instance when nighttime sleep is disrupted by frequent breathing pauses. In other cases, however, hypersomnia occurs even when nighttime sleep is of good quality. These cases of hypersomnia are presumed to be a symptom of brain dysfunction, and so are referred to as hypersomnias of central (i.e., brain) origin. The causes of most of these central hypersomnias are not known. However, our group has recently identified a problem with the major brain chemical responsible for sedation, known as GABA. In a subset of our hypersomnia patients, there is a naturally-occurring substance that causes the GABA receptor to be hyperactive. In essence, it is as though these patients are chronically medicated with Valium (or Xanax or alcohol, all substances that act through the GABA system), even though they do not take these medications. Current treatment of central hypersomnias is limited. For the fraction of cases with narcolepsy, there are FDA-approved, available treatments. However, for the remainder of patients, there are no treatments approved by the FDA. They are usually treated with medications approved for narcolepsy, but sleep experts agree that these medications are often not effective for this group of patients. Based on our understanding of the GABA abnormality in these patients, we evaluated whether clarithromycin (an antibiotic approved by the FDA for the treatment of infections) would reverse the GABA abnormality. In a test tube model of this disease, clarithromycin does in fact return the function of the GABA system to normal. The investigators have treated a few patients with clarithromycin and most have felt that their hypersomnia symptoms improved with this treatment. To determine whether clarithromycin is truly beneficial for central hypersomnia, this study will compare clarithromycin to an inactive pill (the placebo). All subjects will receive both clarithromycin and the placebo at different times, and their reaction times and symptoms will be compared on these two treatments to determine if one is superior. If this study shows that clarithromycin is more effective than placebo in the treatment of hypersomnia, it will identify a potential new therapy for this difficult-to-treat disorder.

Eligibility Criteria

Inclusion Criteria

  • Hypersomnia (meeting clinical criteria for Idiopathic hypersomnia with or without long sleep time, narcolepsy lacking cataplexy, or symptomatic hypersomnia not meeting ICSD criteria)
  • evidence for GABA-related abnormality, as demonstrated by in-house, in vitro assay
  • age > 18
  • high performance liquid chromatography/liquid chromatography tandem mass spectrometry verification of the absence of exogenous benzodiazepines

Exclusion Criteria

  • Contraindications to use of clarithromycin (pregnancy, severe renal impairment, history of QT prolongation, hypomagnesemia, hypokalemia, bradycardia, history of myocardial infarction or cardiomyopathy, myasthenia gravis, age > 70)
  • Current use of cisapride, pimozide, astemizole, terfenadine, colchicines, and ergotamine or dihydroergotamine
  • Current use of benzodiazepines or benzodiazepine-receptor agonists
  • moderate or severe sleep apnea (RDI > 15/hr), severe periodic limb movement disorder (PLMI > 30/hr)
  • diagnosis of narcolepsy with cataplexy, as determined by cerebrospinal hypocretin levels
  • metabolic disorders such as anemia, severe iron deficiency, B12 deficiency, or hypothyroidism that may explain symptoms of hypersomnia
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01146600). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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