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Effects of Xanthohumol on Resting Energy Expenditure and Substrate Oxidation in Healthy Women

U

University of Bonn

Status

Completed

Conditions

Resting Energy Expenditure

Treatments

Dietary Supplement: Placebo
Dietary Supplement: micellar solubilized Xanthohumol

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to investigate the effects of Xanthohumol on resting energy expenditure and substrate oxidation in healthy women. It is assumed that resting energy expenditure and fatty acid oxidation is higher after Xanthohumol ingestion.

Full description

In a crossover design, 16 healthy young women ingest 172 mg micellar solubilized Xanthohumol or placebo in a randomized fashion. During an observational period of 3 hours, the acute effects of Xanthohumol on the resting energy expenditure and substrate oxidation is determined by respiratory gas analysis. An additional 30-minute determination of the resting energy expenditure and substrate oxidation is executed 24 hours after Xanthohumol ingestion. The wash-out period will be 28 days.

Enrollment

16 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • BMI: 18,5 - 24,9 kg/m2
  • metabolically healthy
  • written consent

Exclusion criteria

  • smoking
  • low or high blood pressure
  • dyslipidemia
  • insulin resistance or diabetes mellitus type 1 or type 2
  • gastrointestinal diseases (e.g. food intolerances or allergies)
  • liver, kidney and/or thyroid diseases
  • hepatitis B or C, HIV Infection
  • chronic inflammatory diseases
  • disordered eating
  • psychological diseases
  • alcohol and/or drug abuse
  • use of medication
  • pregnancy or lactating
  • participation in another intervention study
  • irregular menstrual cycle
  • more than 6 hours of sports per week

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

16 participants in 2 patient groups, including a placebo group

Xanthohumol
Experimental group
Description:
single dose of 172 mg of micellar solubilized Xanthohumol
Treatment:
Dietary Supplement: micellar solubilized Xanthohumol
Placebo
Placebo Comparator group
Description:
Polysorbat 80 (E433)
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Central trial contact

Sarah Egert, Prof PhD; Marit Casten, M.Sc.

Data sourced from clinicaltrials.gov

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