Actively Recruiting
Investigating the Impact of the Seaweed Derived Food Additive, Carrageenan, on the Human Gut Microbiome
Led by University of Reading · Updated on 2024-12-17
99
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
Sponsors
U
University of Reading
Lead Sponsor
C
Cargill R&D Centre Europe, Havenstraat 84, 1800 Vilvoorde, Belgium
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this study is to investigate whether a seaweed derived food additive, carrageenan, has an impact on the human gut microbiome in vivo. The primary purpose is to assess whether consumption of a carrageenan containing product for 4 weeks can alter the bacterial composition of the gut microbiome in healthy individuals and whether the addition of a prebiotic fibre, inulin, to the product has an enhanced beneficial impact of the gut composition. The main questions to answer are: Does the consumption of a confectionary item containing carrageenan and inulin lead to a positive impact on the faecal microbial community when compared to the confectionary item containing no carrageenan and no inulin (placebo)? Participants will be asked to consume 2 gummy sweets for 4 week period and provide stool and urine samples on 3 occasions over a 9 week period. Does the consumption of a confectionary item containing carrageenan and inulin improve gastrointestinal comfort measured using overall SHS-GI score when compared to baseline measurements recorded during run in period?
CONDITIONS
Official Title
Investigating the Impact of the Seaweed Derived Food Additive, Carrageenan, on the Human Gut Microbiome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy individuals aged 18 to 55 years
You will not qualify if you...
- Prescribed antibiotics in the last 3 months
- Individuals with any gut disorders such as IBS or IBD
- Individuals with any food allergies or intolerances
- Individuals who regularly consume prebiotic or probiotic supplements
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Reading
Reading, Reading, United Kingdom, rg66ah
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
3
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