Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07105514

Indole-3-PROpionic Acid Clinical Trials - a Pilot Study Part 2

Led by Glostrup University Hospital, Copenhagen · Updated on 2025-08-08

32

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

Sponsors

G

Glostrup University Hospital, Copenhagen

Lead Sponsor

U

University of Copenhagen

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this trial is to investigate the biological effects of oral supplementation with indole-3-propionic acid (IPA) taken twice daily in healthy adults. The main scientific questions are: * Does supplementation with IPA increase the abundance of regulatory T cells in the blood? Regulatory T cells are believed to play an important role in preventing autoimmune diseases. * Does supplementation with IPA increase the concentration of brain-derived neurotrophic factor (BDNF) in the blood? BDNF is believed to play an important role in maintaining brain health. * Does supplementation with IPA affect blood analyses commonly performed to assess the risk of metabolic disorders like type 2 diabetes and cardiovascular diseases? Participants will: * Take capsules to achieve a total daily dose of 1000 mg of IPA or placebo: 500 mg every morning and 500 mg every evening for 14 days. * Visit the clinic at the beginning (day 1) and at the end (day 15) of the supplementation period to deliver blood, urine and fecal samples, have simple measurements performed, fulfil questionnaires and report any side effects.

CONDITIONS

Official Title

Indole-3-PROpionic Acid Clinical Trials - a Pilot Study Part 2

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy women and men aged 18 to 65 years
  • Mentally and physically able to participate
Not Eligible

You will not qualify if you...

  • Diagnosis of gut-, heart-, liver-, kidney- or immune-related disorders
  • Use of antibiotics within the last month
  • Pregnancy, lactation, or childbirth within the last five months
  • Use of prescription medication

AI-Screening

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Trial Site Locations

Total: 1 location

1

Optic Neuritis Clinic, Danish Multiple Sclerosis Center, Department of Neurology, Copenhagen University Hospital, Rigshospitalet-Glostrup

Glostrup Municipality, Denmark, 2600

Actively Recruiting

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Research Team

M

Moschoula Passali, MSc, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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