The purpose of the study is to determine if an oral ketone beverage is safe and well-tolerated during moderate intensity exercise in participants with long-chain fatty acid oxidation disorders and if it will raise blood ketones to levels similar to that reported among normal healthy subjects.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Adverse Events- incidence
Timeframe: 2 hours after product intake
Adverse Events- type
Timeframe: 2 hours after product intake
Adverse Events- severity
Timeframe: 2 hours after product intake
Adverse Events- causal relationship
Timeframe: 2 hours after product intake
Abdominal discomfort
Timeframe: 2 hours after product intake
Decreased appetite
Timeframe: 2 hours after product intake
Gastric reflux
Timeframe: 2 hours after product intake
Nausea
Timeframe: 2 hours after product intake
Diarrhea
Timeframe: 2 hours after product intake
Headache
Timeframe: 2 hours after product intake