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The Effects of the Bile Acid Supplement, 7-keto Lithocholic Acid, on Human Gut Microbiota and Risk Factors for Disease.

Sponsor: University of Reading

NCT ID: NCT07499414

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
7-KLCA (supplement), Maltodextrin (supplement)
How long the study runs
Study runs about 20 months (dates as stated)
About the drug or intervention
7-KLCA — supplement: This study will be conducted as a 16 week duration parallel study. · Maltodextrin — supplement: This study will be conducted as a 16 week duration parallel study.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years to 65 Years
Who
All
Number of participants
40
Started
2026-04-06
Last checked
2026-03

Plain English Summary

What is this study?

  • • Testing a new treatment for healthy
  • • NA - 40 participants
  • • In humans and most mammals, bile acids play a role in the metabolism of glucose and the transport and absorption of lipids (such as cholesterol and triglycerides), vitamins, and nutrients by allowing for emulsification (mixing) and absorption of fatty molecules that are consumed

Who can take part?

  • • Ages 18 Years to 65 Years
  • • Diagnosed with healthy

Where?

  • • Reading - Hugh Sinclair Unit, Harry Nursten Building, University of Reading, Whiteknights Campus, RG6 6UR

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

In humans and most mammals, bile acids play a role in the metabolism of glucose and the transport and absorption of lipids (such as cholesterol and triglycerides), vitamins, and nutrients by allowing for emulsification (mixing) and absorption of fatty molecules that are consumed. More recently, bile acids have been discovered to influence the composition and quantity of the microorganisms in the gut microbiome. Bile acids also act as signalling molecules (like hormones) in the body, regulating important metabolic pathways and digestion. While the majority of bile acids are recycled back to the liver, a small proportion of these bile acids enter the colon and interact with the gut microbiota. Primary bile acids, synthesized in the liver, are essential for the absorption of fat- and fat-soluble vitamins, as part of the digestive process. These primary bile acids are converted to secondary bile acids by gut bacteria, which have been shown to have benefits to health. This provides the rationale for exploring the use of a bile acid, in this case 7-keto lithocholic acid (7-KLCA), as a beneficial modulator of the gut microbiome, to help regulate metabolic and potentially other disease pathways.

More detail

Bile acids are small, naturally occurring molecules that play a vital role in the metabolism of glucose and lipids. Bile acids are classified as primary or secondary. Primary bile acids are made from cholesterol in the liver, where they form bile salts and are transported into the gall bladder before finally being secreted into the stomach, as part of the digestive process. \~95% of bile acids are recycled back to the liver, but a small proportion enters the colon and interacts with our gut microbiome. In the gut, these primary bile acids are converted to secondary bile acids (by our gut bacteria), and act as secondary signalling molecules that can affect health. Recent discoveries show that bile acids directly affect the gut microbiome. In fact, ursodeoxycholic acid (UDCA), a secondary bile acid, has a long history in medicine. Though currently used to treat liver diseases, treatment with UDCA has been found to increase the beneficial bacteria Faecalibacterium prausnitzii and reduce levels of hydrogen- and methane-producing bacteria in the gut. Therefore, there is potential to use UDCA (and UDCA-like molecules) as a prebiotic-like molecule that can be used by our gut microorganisms to promote beneficial bacteria in the gut and lead to a health benefit. The bile acid 7-keto lithocholic acid (7-KLCA) is metabolised in the gut to produce UDCA. Using our in vitro fermentation models, UDCA and 7-KLCA were evaluated and found to increase the incidence of the beneficial microorganisms: Lactobacillus, Eubacterium rectale and Bifidobacterium spp. Changes in downstream bacterial metabolites and increases in short chain fatty acids also were observed. Our in vitro fermentation results, coupled with our in vitro cell culture studies, suggest there may be additional mechanisms by which UDCA and UDCA-like molecules exert their beneficial effects. This study aims to assess in vivo, via a human intervention study, the prebiotic potential of 7-KLCA, as a bile acid supplement, and how microbial changes in the gut can improve biomarkers, indicative of beneficial metabolic and microbiome function and reduce risk factors of disease. In preparation for this study, 7-KLCA has undergone toxicology, absorption, and bioavailability studies to ensure it is safe for human consumption. Blood faecal and urine samples will be obtained at key points in the study, to assess microbial changes (bacterial count and composition, as well as metabolite profiling analysis; fatty acid, bile acid and lipids) and monitor key biomarkers (blood glucose and cholesterol, and indicators of inflammation and immune response), to address our primary and secondary research questions.

Healthy

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 65 Years
  • Who can join: All genders

What the study is looking for

  • ✓Volunteer is healthy (good physical and mental condition, disease-free, with haemoglobin levels between 138 - 172...
  • ✓Volunteer is aged ≥ 18 to ≤ 65 years for the duration of the study
  • ✓Volunteer is able and willing to comply with the study instructions
  • ✓Volunteer is suitable for participation in the study according to the investigator/study personnel
  • ✓Volunteer is able to give agreement to take part

Who cannot take part

  • ✗No command of any local language
  • ✗Gastrointestinal disorders including IBS, IBD or other conditions that might affect the gut environment
  • ✗Food allergies or intolerances
  • ✗Using drugs (e.g. antibiotics) influencing gastrointestinal function (12 weeks before intervention)
  • ✗Use of laxatives
See the full criteria
Inclusion Criteria: * Volunteer is healthy (good physical and mental condition, disease-free, with haemoglobin levels between 138 - 172 g/L for male and between 121 and 151 g/L for female) at the time of pre-examination * Volunteer is aged ≥ 18 to ≤ 65 years for the duration of the study * Volunteer is able and willing to comply with the study instructions * Volunteer is suitable for participation in the study according to the investigator/study personnel * Volunteer is able to give informed consent * Volunteer must be following a non-restrictive diet according to the investigator/study personnel (no vegan, keto or fasting diets) * Volunteer has not consumed pro- or prebiotic supplements or food products for a minimum of 4 weeks prior to starting the intervention. * Volunteer has no gastrointestinal disorders Exclusion Criteria: * No command of any local language * Gastrointestinal disorders including IBS, IBD or other conditions that might affect the gut environment * Food allergies or intolerances * Using drugs (e.g. antibiotics) influencing gastrointestinal function (12 weeks before intervention) * Use of laxatives * Clinically significant diabetes (plasma glucose test, fasting blood glucose \> 6.5 mmol/l (120 mg/dL) * Volunteers currently involved or will be involved in another clinical/ food study for the duration of this study * History of drug (pharmaceutical or recreational) or alcohol abuse. * If participants are pregnant or are lactating * Regular intake of probiotic or prebiotic supplements * Smoker * Those who follow extreme diets (Keto-diet, Atkins diet, vegan) * Those taking prescribed medication for existing health condition(s) * Those with a pacemaker

Where Is This Study? (1 UK site)

Hugh Sinclair Unit, Harry Nursten Building, University of Reading, Whiteknights Campus, RG6 6UR

Reading, United Kingdom

Recruiting
Site contact (verified)
Kimberly Watson, DPhilPrincipal Investigator

How to Get in Touch

Abigail Basson, PhD

Sponsor contact

CONTACT

+44(0)7756872508 biomet-7@reading.ac.uk

Kimberly Watson, DPhil

Sponsor contact

CONTACT

+44(0)1183786640 biomet-7@reading.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-03