Combination Upper-Airway Electrical and Pharmacological Stimulation for Obstructive Sleep Apnea

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-79
SponsorBrigham and Women's Hospital

About this trial

Obstructive sleep apnea (OSA) is a common condition in which the airway repeatedly collapses during sleep, leading to poor sleep quality and reduced oxygen levels. Hypoglossal nerve stimulation (HGNS) is an approved treatment that uses a small implanted device to stimulate the genioglossus muscle and keep the airway open. However, some patients continue to have OSA despite using HGNS. Atomoxetine and oxybutynin, "AtoOxy", is a promising pharmacologcal therapy under investigation that has been shown to activate pharyngeal muscles-in particular non-genioglossus muscles--but appears more efficacious in some patients than others.

This study will test whether the combination of AtoOxy and HGNS can further improve breathing during sleep compared to either monotherapy alone. Participants with OSA and an HGNS device will be randomized to receive, in random order: HGNS+AtoOxy, HGNS alone (plus placebo), AtoOxy alone (HGNS device off), and placebo (HGNS device off), in a cross-over trial.

The main goal is to determine whether the combined treatment reduces the number of breathing events during sleep; the primary outcome test will compare HGNS+AtoOxy versus HGNS alone. The effect of each intervention versus placebo will also be presented.

The study will also examine how individual patient characteristics influence response to treatment.

Eligibility criteria

Qualifiers

Ages 18 - 79 years

Diagnosed OSA

Implantation of a hypoglossal nerve stimulation device (HGNS, Inspire Medical) or scheduled for implantation (implantation required for randomization)

Willingness to withhold HGNS while testing therapies (up to 6 weeks with HGNS off [with/without pharmacotherapy] to assess benefits of HGNS therapy).

Disqualifiers

Any uncontrolled medical condition

Current use of the medications under investigation.

Issues relating to short-term withdrawal of HGNS therapy

Excluded: Occupational driving (truck drivers, fork-lift operation, taxi/uber drivers)

Trial design

Treatments tested in this trial

  • Combination device and drug: Unilateral hypoglossal nerve stimulation & atomoxetine-plus-oxybutynin (HGNS+AtoOxy)
  • Unilateral hypoglossal nerve stimulation (HGNS), active comparator condition
  • Atomoxetine-plus-oxybutynin (80/5 mg) (AtoOxy), active comparator condition
  • Placebo; placebo comparator condition

Treatment groups

24 Participants
are divided into 4 treatment groups

Sponsors and collaborators