Summary

Eligibility
for people ages 21 years and up (full criteria)
Location
at UCLA
Dates
study started
completion around
Principal Investigator
by Eric Kezirian, MD, MPH (ucla)

Description

Summary

This study will examine factors associated with outcomes after soft palate surgery and medications (acetazolamide, eszopiclone) that may treat other potential causes of obstructive sleep apnea (loop gain, arousal threshold).

Details

This is a prospective cohort (observational) study of 150 participants with moderate to severe obstructive sleep apnea (OSA) unable to tolerate positive airway pressure who are undergoing drug-induced sleep endoscopy (DISE), including measurement of upper airway closing pressure (Pclose), and tissue-repositioning soft palate surgery. Before and 6 months after surgery, the investigators will measure OSA severity (apnea-hypopnea index) with sleep studies (polysomnograms). Using a recently-validated polysomnography-based signal processing algorithm, the investigators will systematically assess the underlying mechanisms of OSA (traits) and airflow shape (consistent with palate obstruction). The expected 90 participants without resolution of OSA after surgery (surgery failures) will participate in an experimental randomized crossover study of acetazolamide (1 month) and acetazolamide/eszopiclone combination (1 month). Polysomnograms will be performed with each treatment, with algorithm-based determination of traits.

Keywords

Obstructive Sleep Apnea, surgery, loop gain, arousal threshold, Apnea, Sleep Apnea Syndromes, Acetazolamide, Eszopiclone, Acetazolamide 500 MG QHS, Eszopiclone 3 mg QHS, Acetazolamide/Eszopiclone

Eligibility

You can join if…

Open to people ages 21 years and up

are:

  1. age ≥21 years;
  2. moderate to severe OSA (obstructive AHI ≥ 15 events/hour);
  3. central/mixed apnea index <5 events/hour;
  4. intolerance of positive airway pressure (defined as use < 2 hours/night at least 5 nights/week);
  5. intolerance or poor candidate for oral appliance;
  6. participant has provided informed consent for palate surgery as part of their standard of care;
  7. tonsil size 0-2+ (without markedly enlarged tonsils that have high surgical success rates);
  8. DISE without evidence of complete tongue-related obstruction (reflecting poorer results with isolated palate surgery);
  9. medications stable for ≥2 months;
  10. body mass index <35 kg/m2;
  11. absence of uncontrolled nasal obstruction;
  12. no prior pharyngeal surgery other than tonsillectomy;
  13. no neurologic, cardiac or pulmonary disorders;
  14. absence of psychiatric disorder except for treated depression or mild anxiety;
  15. no co-existing sleep disorder, such as narcolepsy, chronic insomnia, or restless legs syndrome;
  16. no use of hypnotics, anxiolytics, stimulants, or sedating antidepressants;
  17. no near-miss or prior motor vehicle crash due to sleepiness in past 12 months; and
  18. <3 caffeinated beverages daily.

You CAN'T join if...

are:

  1. history of allergic reaction to either of the study drugs;
  2. subjects with prior serious allergic reaction (such as Stevens-Johnson syndrome) to sulfonamides;
  3. subjects with a history of hypersensitivity to either of the two study drugs;
  4. subjects who are on high-dose aspirin therapy due to risk of severe metabolic acidosis;
  5. subjects with severe kidney disease or severe liver disease;
  6. subjects with a history of electrolyte imbalance or adrenal insufficiency (due to risks related to acetazolamide);
  7. subjects on ketoconazole or other strong CYP3A4 inhibitors (these will increase eszopiclone blood levels);
  8. pregnancy; and
  9. alcohol or substance abuse.

Locations

  • UCLA Santa Monica Medical Center accepting new patients
    Santa Monica California 90401 United States
  • UCLA Westwood not yet accepting patients
    Westwood California 90095 United States

Lead Scientist at University of California Health

  • Eric Kezirian, MD, MPH (ucla)
    Eric Kezirian has a clinical and research focus in the surgical evaluation and treatment of obstructive sleep apnea and snoring.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Los Angeles
ID
NCT05953610
Phase
Phase 2 research study
Study Type
Interventional
Participants
Expecting 150 study participants
Last Updated