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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05711212
Enrollment
16
Registered
2023-02-02
Start date
2023-02-15
Completion date
2024-04-30
Last updated
2024-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Resting Energy Expenditure

Keywords

Xanthohumol, micellar solubilization, fatty acid oxidation

Brief summary

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.

Detailed 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.

Interventions

DIETARY_SUPPLEMENTmicellar solubilized Xanthohumol

single administration of 4 soft gelatine capsules each containing 43 mg micellar solubilized Xanthohumol

DIETARY_SUPPLEMENTPlacebo

single administration of 4 soft gelatine capsules containing only micelles

Sponsors

University of Bonn
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Prolonged Effect on Substrate Oxidationassessed uninterrupted for 30 minutes 24 h post doseassessed by the respiratory quotient (RQ=VCO2/VO2), given in percent
Acute Effect on Resting Energy Expenditureassessed uninterrupted for 3 hours post dosecalculated from Volume of inhaled oxygen (VO2) in L/min and exhaled carbon dioxide (VCO2) in L/min, given in kcal/24 hours
Prolonged Effect on Resting Energy Expenditureassessed uninterrupted for 30 minutes 24 h post dosecalculated from Volume of inhaled oxygen (VO2) in L/min and exhaled carbon dioxide (VCO2) in L/min, given in kcal/24hours
Acute Effect on Substrate Oxidationassessed uninterrupted for 3 hours post doseassessed by the respiratory quotient (RQ=VCO2/VO2), given in percent

Secondary

MeasureTime frameDescription
Acute Effect on Blood pressure0, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180 minutes post dosegiven in millimeter mercury
Prolonged Effect on Blood pressure24 hours, 24 hours and 10 minutes, 24 hours and 20 minutes, 24 hours and 30 minutes post dosegiven in millimeter mercury
Acute Effect on Pulse0, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180 minutes post dosegiven in beats per minute
Prolonged Effect on Pulse24 hours, 24 hours and 10 minutes, 24 hours and 20 minutes, 24 hours and 30 minutes post dosegiven in beats per minute

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026