150
Participants
Start Date
May 2, 2019
Primary Completion Date
December 31, 2026
Study Completion Date
March 31, 2027
Hyperoxia
The ventilatory effects of brief hyperoxia will be assessed by analyzing control breaths on room air immediately preceding the hyperoxic exposure, and comparing with the primary end-point, nadir minute ventilation breath, immediately following the brief hyperoxic exposure.
Acetazolamide
Participants with sleep apnea will ingest capsules containing either placebo or acetazolamide 500 mg twice a day for 6 days. On the final 4 consecutive nights while still on ACZ, the investigators will perform i) physiology tests and ii) in-lab follow-up PSG.
RECRUITING
John D. Dingell VA Medical Center, Detroit, MI, Detroit
John D. Dingell VA Medical Center
FED
VA Office of Research and Development
FED