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COMPLETED
NCT06053138
NA

Assessment of BHB Concentration Agreement Among Sampling Locations and the Impact of Ketosis on EPO, and More

Sponsor: Central Jutland Regional Hospital

View on ClinicalTrials.gov

Summary

This study aims to address two key aspects. First, the suitability of selecting a specific sampling site for BHB measurement in patients and research, as well as potential differences between capillary and venous blood measurements. Additionally, the study will investigate the effects of ketosis on EPO concentrations, sex hormone levels, hemodynamic markers, and blood pressure. This investigation will utilize blood samples collected from baseline and at Day 15, between which participants are exposed to intermittent ketosis or placebo in a randomized parallel design.

Official title: Assessment of BHB Concentration Agreement Among Sampling Locations and the Impact of Ketosis on Erythropoietin Levels: A Two-Part Study

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

16

Start Date

2023-08-24

Completion Date

2024-08-30

Last Updated

2026-04-28

Healthy Volunteers

Yes

Conditions

Interventions

DIETARY_SUPPLEMENT

Ketone monoester

Supraphysiological ketosis induced by ingestion of a ketone monoester dietary supplement administered intermittently during the randomized two-week intervention period.

DIETARY_SUPPLEMENT

Placebo

The placebo vehicle is matched to the ketosis intervention in the experimental arm with regards to taste, volume, viscosity, appearence, and packaging

Locations (1)

Department of Internal Medicine, Viborg Regional Hospital

Viborg, Denmark