Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07452562

Hesperidin RCT in MS

Led by Swansea University · Updated on 2026-03-05

60

Participants Needed

1

Research Sites

53 weeks

Total Duration

On this page

Sponsors

S

Swansea University

Lead Sponsor

B

BioActor B.V.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is a randomised, double-blind, placebo-controlled trial investigating the effects of Hesperidin supplementation on cognitive function, fatigue, and stress. Participants will be randomly assigned to receive either 500mg of Hesperidin or a matching placebo daily for 12 weeks. The primary outcome is fatigue, with secondary outcomes including cognitive performance and mood. The trial seeks to determine if this dietary intervention offers symptom-alleviating benefits.

CONDITIONS

Official Title

Hesperidin RCT in MS

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Multiple Sclerosis
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Known food allergies, intolerances, or significant gastrointestinal (GI) problems
  • Participants under the age of 18 years

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

FHMLS, Nutrition Lab

Swansea, Wales, United Kingdom, SA2 8PP

Actively Recruiting

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Research Team

H

Hayley Young, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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