Impact of Exogenous Ketones on Sleep Apnea

PHASE1/PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

September 6, 2026

Primary Completion Date

September 6, 2028

Study Completion Date

September 6, 2028

Conditions
Obstructive Sleep ApneaSleep
Interventions
DIETARY_SUPPLEMENT

Ketone-IQ

This is a crossover study where participants will ingest either Ketone-IQ for 2 nights, or placebo for 2 nights before sleep. This is the Ketone-IQ (1,3 Butanediol) intervention.

DIETARY_SUPPLEMENT

Placebo

This is a crossover study where participants will ingest either Ketone-IQ for 2 nights, or placebo for 2 nights before sleep. This is the Placebo intervention.

Trial Locations (1)

21224

Johns Hopkins Bayview Medical Center, Baltimore

All Listed Sponsors
collaborator

HVMN Inc

INDUSTRY

collaborator

KETONE-IQ

UNKNOWN

lead

Johns Hopkins University

OTHER