Clinical Trials in Switzerland / NCT06134258
Recruiting Not applicable

Mechanisms of Fasting Induced Reduction in Energy Expenditure

NCT06134258 · tracked via the Priya Life Science Switzerland tracker
Sponsor
Phase
Not applicable
Started
2023-11-15
Last updated
2025-05-30

Condition(s) studied

Fasting

Investigational drug(s) / intervention(s)

mixed meal test

mixed meal test: mixed meal test after fasting

Study summary

Fasting reduces the energy consumption of the human body. The extent of this adaptation varies significantly between different individuals. The aim of this research project is to investigate how this adaptation of the metabolism is regulated by the body. For this purpose, we will first measure how the so-called basal metabolic rate of the body reacts to a short-term fasting of 24 h in a preliminary study. Those subjects with a particularly pronounced and those subjects with an only slightly pronounced reaction of the basal metabolic rate will be invited to the main study.

Here, in random order (24 h fasting vs. 8 h fasting), the following is compared

* how the basal metabolic rate of the body reacts to the reduced energy intake.
* how the energy metabolism increases after a test meal
* what role in particular the thyroid hormones play in this adaptation. In addition, a sample of the subcutaneous adipose tissue is taken in each case and it is examined how the regulation of metabolic processes at the cellular level.

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age: 18 to 40 years * Body mass index 18.0 to 27.0 kg/m² * Exclusion Criteria: * Chronic conditions necessitating medical treatment (e.g., renal failure, hepatic dysfunction, cardiovascular disease, diabetes mellitus), * Known or suspected non-compliance, drug or alcohol abuse, * Inability to follow the procedures of the study * Participation in another study with investigational drug within the 30 days preceding and during the present study, * Previous enrolment into the current study, * Enrolment of the investigator, his/her family members, employees and other dependent persons, * Hypothyroidism or hyperthyroidism * Pregnant, breastfeeding and menopausal women

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Basel Basel Switzerland Recruiting

More ETH Zurich trials in Switzerland

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06134258 on ClinicalTrials.gov ↗ ← All trials in Switzerland