RecruitingPhase 2NCT06521476

Acetazolamide in Central Sleep Apnea Patients Using Medication for Opioid Use Disorder

Impact of Acetazolamide on Central Sleep Apnea Patients Receiving Medication for Opioid Use Disorder


Sponsor

Sanjay R Patel

Enrollment

40 participants

Start Date

Sep 30, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Patients with opioid use disorder treated with either methadone or buprenorphine are at risk of developing central sleep apnea (CSA) from these medications. Investigators will conduct a mechanistic trial using acetazolamide, a medicine known to improve CSA in other settings, to determine if acetazolamide can improve CSA due to medication for opioid use disorder and whether this leads to physiologic changes that might lead to reduced drug craving. Patients treated with medication for opioid use disorder and who have central sleep apnea will be randomized to treatment with acetazolamide or matching placebo for 7 days. At the end of the 7 days, they will undergo an overnight sleep study to assess the impact on breathing during sleep as well as sleep quality. In addition, measures of sympathetic tone, anxiety, arousal, cognition, and drug craving will be measured to determine if treatment of CSA with acetazolamide can produce physiologic changes that might contribute to improved health.


Eligibility

Min Age: 18 YearsMax Age: 100 Years

Inclusion Criteria1

  • Patients on Medication for Opioid Use Disorder (MOUD) with central sleep apnea.

Exclusion Criteria4

  • Sleep-related Hypoventilation.
  • Other causes of Central Sleep Apnea besides Opioid Use.
  • Pregnancy.
  • Contraindications for Acetazolamide.

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Interventions

DRUGAcetazolamide

Oral acetazolamide 250 mg daily for 7 days

DRUGPlacebo

Oral placebo daily for 7 days


Locations(1)

University of Pittsburgh

Pittsburgh, Pennsylvania, United States

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NCT06521476