Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT06981663

Effects of Fibres Combined With Probiotics on Uric Acid in an ex Vivo Fermentation Model

Led by Örebro University, Sweden · Updated on 2025-08-12

15

Participants Needed

1

Research Sites

181 weeks

Total Duration

On this page

Sponsors

Ö

Örebro University, Sweden

Lead Sponsor

U

University of Copenhagen

Collaborating Sponsor

AI-Summary

What this Trial Is About

In this study, we will collect faecal samples from individuals with hyperuricaemia (assessed by blood test) and perform in vitro faecal fermentation studies to assess how probiotics in combination with fibres affect urate metabolism in these faecal samples.

CONDITIONS

Official Title

Effects of Fibres Combined With Probiotics on Uric Acid in an ex Vivo Fermentation Model

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent before any study procedures
  • Age between 18 and 80 years
  • Body Mass Index (BMI) between 18.5 and 35 kg/m2
  • Blood uric acid level above 0.36 mmol/L (6 mg/dl)
  • Willing to avoid regular use of probiotic supplements or probiotic-containing foods until stool collection
  • Willing to avoid regular use of supplements or medications that affect gut function or inflammation until stool collection
Not Eligible

You will not qualify if you...

  • Diagnosed with type 1 or type 2 diabetes
  • Diagnosed with inflammatory bowel disease (IBD)
  • Currently diagnosed with psychiatric diseases or syndromes
  • Currently diagnosed with neurodegenerative diseases
  • Currently pregnant or breastfeeding
  • History of complicated gastrointestinal surgery
  • Used systemic antibiotics or steroid medications within the last 4 months
  • Regular use of non-steroidal anti-inflammatory drugs (NSAIDs) in the last 2 months
  • Taken any NSAIDs within 3 days before sample collection
  • Used probiotic supplements within 4 weeks prior to study start
  • Any condition or medication use that could affect study results, as judged by the principal investigator
  • Starting any new medication or treatment that might impact participation or analysis after study inclusion and before stool collection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Örebro University

Örebro, Sweden

Actively Recruiting

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Research Team

J

Julia König, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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