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Ketone Supplementation in Individuals With PTSD

NCT04083352 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2019-11-18

No results posted yet for this study

Summary

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.

Conditions

Interventions

DIETARY_SUPPLEMENT

Pruvit Ketomax Ketone Salt

6-week supplementation with ketone salts

DIETARY_SUPPLEMENT

Placebo

Placebo was taken for 6-weeks and was calorie and flavor matched to the ketone salt supplement.

Sponsors & Collaborators

  • Augusta University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-30
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04083352 on ClinicalTrials.gov