Skip to main content
OpenTrials
Completed

NCT Number: NCT05980858

Effects of Exogenous Ketosis on Renal Function, Renal Perfusion, and Sodium Excretory Capacity in Healthy Subjects

This is a randomized, placebo-controlled, double-blinded crossover design. Fifteen healthy subjects will be randomized to receive either ketone bodies (KE4) or placebo delivered by KetoneAid. After a period of 5-days treatment, effect variables will be measured (experiment day 1). After a washout period of 14 days, the subjects are crossed over to a similar treatment period with the other treatment. The study is terminated by measuring effect variables after the second treatment period (experiment day 2).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University Clinic of Nephrology and Hypertension

Herning, Jutland, 7400, Denmark

About this study

Background: Renewed interest in ketone bodies has emerged, partly driven by the recent success of selective sodium glucose co transporter 2 (SGLT-2) inhibition in preventing cardiovascular deaths in patients with diabetes mellitus (DM) and chronic kidney disease (CKD). Effects of ketosis are of importance in order to understand the beneficial effects of SGLT-2 inhibitors and to account for the full therapeutic potential of this treatment.

Hypothesis: Ketosis increases renal blood flow and glomerular filtration rate (GFR).

Methods: It is a randomized, placebo-controlled double-blinded cross over study. Fifteen healthy subjects will be randomized to receive either ketone bodies (KE4) or for 5 days. After a wash out period of at least 14 days, the subjects are crossed over to receive the other treatment. After each treatment period effect variables will be measured including Technetium(Tc)99m - Diethylenetriamine pentaacetate (DTPA) clearance and water based positron emission tomography computed tomography (PET/CT)

Perspectives: The study has the potential to provide information regarding the therapeutic potential of treatment with ketone bodies and understanding of conditions characterized by ketosis, such as SGLT2-inhibitor treatment.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI < 30 kg/m2
  • Safe contraception if women in childbearing age
  • Normal biochemical screening

Exclusion criteria

  • Pregnancy or breast feeding
  • Major heart-, liver-, kidney-, lung-, neurological- or endocrine disease
  • Daily use of prescription drugs (expect for contraceptives)
  • Alcohol or drug abuse
  • Periodic fasting
  • Routinely intake of ketogenic diet

Treatment and study plan

Beta-Hydroxybutyrate

Dietary Supplement

Each subject receive Beta-hydroxybutyrate 300mg/kg x 3 for five days. After the treatment period effect variables will be examined.

Placebo

Other

Each subject receive a placebo drink 3 x day for five days. After the treatment period effect variables will be examined.

Primary outcomes

  1. GFR

    Time frame: Measured after each treatment period (day 6 and approximately day 26)

    Change in GFR measured by Tc99m-DTPA clearance

  2. Renal Blood Flow (RBF)

    Time frame: Subjects are scanned after each treatment period (day 6 and approximately day 26)

    Change in RBF determined by water based PET/CT scans

Secondary outcomes

  1. 24-hour blood pressure

    Time frame: Measured after each treatment period (day 6 and approximately day 26)

    Change in systolic 24-hour blood pressure

  2. Vasoactive hormones

    Time frame: Measured after each treatment period (day 6 and approximately day 26)

    Change in plasma levels of angiotensin II, aldosterone, renin, brain natriuretic peptide (BNP), atrial natriuretic peptide (ANP), copeptin

  3. Beta-hydroxybutyrate

    Time frame: Measured after each treatment period (day 6 and approximately day 26)

    Change ind p-beta-hydroxybutyrate

  4. Renal tubular transport proteins

    Time frame: Measured after each treatment period (day 6 and approximately day 26)

    Urine excretions of aquaporin 2 (AQP2), thiazide-sensitive sodium-chloride cotransporter (NCC) and distal epithelial sodium channel (ENaC)

Sponsors and collaborators

Lead sponsor

Gødstrup Hospital

Other

Registry information

Acronym: KETO

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Aug 8, 2023
Registry last updated
Nov 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.