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NCT06418074Completed

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

Effects of Exogenous Ketosis on Renal Function, Renal Perfusion, and Sodium Excretory Capacity in Patients With Essential Hypertension

Source: ClinicalTrials.gov · Last updated 10 Dec 2025

Brief summary (registry, in English)

This is a randomized, placebo-controlled, double-blinded crossover design. Nineteen patients with essential hypertension 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).

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
6 May 2024
Start date
11 Sept 2024
Primary completion date
19 Jun 2025
Lead sponsor
Gødstrup Hospital
NCT number
NCT06418074

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 11 Sept 2024 to the primary completion date, 19 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Daily use of prescription drugs (expect for contraceptives)
  • Alcohol or drug abuse
  • Treatment with immunosuppressants or SGLT2-inhibitors

Other illness

  • Diabetes type 1 or 2
  • Heart Failure
  • Liver disease
  • Malignant disease
  • Recent acute myocardial infarction (AMI), apoplexia/transient ischemic attack (TIA) (within 12 months of inclusion)

Other

  • Pregnancy or breast feeding
  • Periodic fasting
  • Routinely intake of ketogenic diet

Who the study is looking for

  • Essential hypertension (treatment with maximum 2 antihypertensive drugs)
  • eGFR \> 60ml/min
  • BMI \< 35 kg/m2
  • Urine Albumin Creatinin Ratio (UACR) \< 300mg/g
  • Safe contraception if women in childbearing age

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University Clinic in Nephrology and Hypertension, Gødstrup Region Hospital
Coordinator of this site? Confirm its status
HerningDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.