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Completed

NCT Number: NCT07250191

The Effects of 24-hour Fasting or Carbohydrate Restriction on Postprandial Metabolic Responses

Most individuals spend the majority of the day in a fed state, making postprandial blood glucose and lipid regulation a central component of metabolic health. Short periods of fasting or reduced carbohydrate intake can occur frequently in daily life, whether through intentional dietary practices (e.g. intermittent fasting), cultural or religious traditions, or unstructured eating patterns. These periods can induce measurable metabolic changes, but the acute effects of a single 24-hour period of fasting or carbohydrate restriction on postprandial metabolism upon refeeding remain poorly characterised.

This study will examine how 24 hours of either complete fasting or low carbohydrate intake without energy restriction influence postprandial blood glucose and lipid concentrations, as well as related metabolic markers, in healthy adults, in comparison to a habitual high carbohydrate control diet. Participants will complete all three conditions in a randomised order, consuming a standardised meal test after each 24-hour condition. Repeated blood sampling and gas exchange measurements will be carried out to assess postprandial metabolic responses.

The aim of this study is to characterise whether acute periods of fasting and low carbohydrate restriction elicit distinct or comparable alterations in postprandial metabolic responses. A clearer understanding of these acute physiological effects can help inform how variations in eating patterns influence glucose and lipid handling in individuals without metabolic disease.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Bath

Bath, BA2 7AY, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged between 18-40 years
  • Have a BMI of 18.5-29.9 kg/m2

Exclusion criteria

  • Diagnosed with any major chronic conditions (e.g. type 2 diabetes, coronary heart disease, cancer, chronic kidney disease, etc.)
  • Use of medication that may interfere with study outcomes (e.g. glucose or lipid-lowering medications)
  • Currently or recently pregnant (within last 6 months), planning to get pregnant or currently lactating
  • Has a habitually low carbohydrate intake (<150g carbohydrates/day)
  • Current or previous eating disorder
  • Has donated more than 500ml of blood in the last 3 months prior to the initial laboratory visit
  • Insufficient mental capacity or language skills to independently understand and follow the study protocol
  • Has an irregular sleeping pattern (e.g. due to undertaking night-shift work)
  • Any other condition, concurrent intervention or behaviour deemed either to pose undue personal risk to the participant or to introduce bias into the experiment

Treatment and study plan

Fasting

Behavioral

No food intake for 24 hours

Carbohydrate restriction

Behavioral

Restriction of dietary carbohydrate to ≤5% of total energy intake for 24 hours

Other names: Ketogenic diet

Primary outcomes

  1. Triglyceride Concentration

    Time frame: After each 24-hour dietary condition

    Plasma triglyceride concentrations assessed at baseline and postprandially for 2 hours after a mixed meal test

  2. Glucose Concentration

    Time frame: After each 24-hour dietary condition

    Plasma glucose concentrations assessed at baseline and postprandially for 2 hours after a mixed meal test

Secondary outcomes

  1. Insulin Concentration

    Time frame: After each 24-hour dietary condition

    Plasma insulin concentrations assessed postprandially for 2 hours after a mixed meal test

  2. Non-esterified Fatty Acid Concentration

    Time frame: After each 24-hour dietary condition

    Plasma non-esterified fatty acid concentrations assessed at baseline and postprandially for 2 hours after a mixed meal test

  3. Beta-hydroxybutyrate Concentration

    Time frame: After each 24-hour dietary condition

    Plasma beta-hydroxybutyrate concentrations assessed at baseline and postprandially for 2 hours after a mixed meal test

  4. Substrate Oxidation

    Time frame: After each 24-hour dietary condition

    Lipid and carbohydrate oxidation assessed via indirect calorimetry at baseline and during 2-hour mixed meal test

Sponsors and collaborators

Lead sponsor

University of Bath

Other

Registry information

Official study title

The Acute Effects of Energy and Carbohydrate Restriction on Postprandial Metabolism

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Nov 26, 2025
Registry last updated
Nov 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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