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RECRUITING
NCT06521476
PHASE2

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

Sponsor: Sanjay R Patel

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - 100 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-09-30

Completion Date

2028-02

Last Updated

2025-10-16

Healthy Volunteers

No

Interventions

DRUG

Acetazolamide

Oral acetazolamide 250 mg daily for 7 days

DRUG

Placebo

Oral placebo daily for 7 days

Locations (1)

University of Pittsburgh

Pittsburgh, Pennsylvania, United States