Ketone Supplementation in Individuals With PTSD

Status unconfirmed · Not applicable · Has a placebo group

Conditions studied: PTSD, Ketosis

In brief

The purpose of this study is to determine if a 6-week period of ketone salt supplementation affects physiological, emotional, cognitive, and/or behavioral health markers in individuals with PTSD.

Key facts

Study ID

NCT04083352

Run by

Augusta University

People needed

24

Starts

2016-08-30

Expected to finish

2019-12-01

Last updated by the study team

2019-11-18

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Diagnosed with PTSD

You may not qualify if…

• Pregnant, younger than 18 or older than 65

Where it is running

• Augusta University — Augusta, Georgia, United States (enrolling)

Full record on ClinicalTrials.gov

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