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Echocardiographic Changes After 3-hydroxy Butyrate+Whey Intake

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University of Aarhus

Status

Completed

Conditions

Cardiac Output
Catabolic State
Echocardiography
Endotoxemia

Treatments

Dietary Supplement: Whey
Dietary Supplement: 3-OHB + Whey

Study type

Interventional

Funder types

Other

Identifiers

NCT04037722
Ketone Heart Study

Details and patient eligibility

About

This study evaluates the cardiovascular effects of adding the ketone body 3-hydroxy butyrate (3-OHB) to whey protein during human endotoxemia. Further, this study compares cardiovascular changes during healthy and catabolic conditions.

Participants will receive isocaloric, isonitrogenous beverages of either whey or 3-OHB+whey in a randomized crossover design during either healthy (overnight fast) or catabolic conditions (inflammation/endotoxemia + 36 h fast and bed rest).

Full description

Background: A newly published study found beneficial cardiovascular effects of 3-OHB infusion in a population with chronic heart failure, significantly increasing cardiac output. Similar effects on cardiac output were observed in healthy volunteers. These findings pave the way for 3-OHB as a therapeutic nutritional supplement, since it is well-absorbed during oral consumption. However, it is unknown whether the cardiovascular effects of 3-OHB persist during a sepsis-like catabolic state and when administered orally.

Aim: This study aims to investigate the cardiovascular effects of adding the ketone body 3-hydroxy butyrate (3-OHB) to whey protein during a human disease model, comprising endotoxemia + bed rest + fast.

Hypothesis:

  1. Adding the ketone body 3-OHB to an oral protein supplement increases cardiac output measures

  2. Catabolic stress (endotoxemia/inflammation + 36 h fast and bed rest) induces cardiovascular changes compared with healthy conditions (overnight fast)

    Interventions:

    In a randomized crossover design, eight healthy, lean, young men will undergo either:

    i) Healthy conditions (overnight fast) + whey protein^

    ii) Catabolic conditions (Inflammation (LPS) + 36-hour fast and bed rest*) + whey protein^

    iii) Catabolic conditions (Inflammation (LPS) + 36-hour fast and bed rest*) + 3-OHB/whey protein^"

    *LPS will be administered (1 ng/kg) the day prior to the study together with fast and bed rest. On the study day LPS (0.5 ng/kg) will be injected.

    ^Beverages will be isonitrogenous and isocaloric (fat will be added) with 45 g whey protein + 20 g maltodextrin. Bolus/sip administration will be applied (1/3 bolus, 1/2 sip)

    " 50 grams of 3-OHB will be orally administered (1/2 bolus, 1/2 sip)

Enrollment

8 patients

Sex

Male

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Between 20-40 years of age
  • Body mass index between 20-30 kg/m^2
  • Healthy
  • Oral and written consent forms obtained prior to study day

Exclusion criteria

  • Recent immobilization of an extremity that is not fully rehabilitated

  • Lactose, lidocain or rubber allergies

  • Current disease

  • Use of anabolic steroids

  • Smoking

  • Former major abdominal surgery (Or current problems with the GI tract)

    •>10 hours of exercise/weak

  • Present ketogenic diets or high-protein diets

  • Blood doner that does not want to discontinue blood donations until study completion

  • Pending MR scan

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

8 participants in 3 patient groups

Healthy + Whey
Experimental group
Description:
Healthy conditions (overnight fast)
Treatment:
Dietary Supplement: Whey
Catabolic + Whey
Experimental group
Description:
Catabolic conditions (36-hour fast, bed rest and inflammation (LPS))
Treatment:
Dietary Supplement: Whey
Catabolic + 3-OHB / Whey
Experimental group
Description:
Catabolic conditions (36-hour fast, bed rest and inflammation (LPS))
Treatment:
Dietary Supplement: 3-OHB + Whey

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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