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Hesperidin RCT in MS

Sponsor: Swansea University

NCT ID: NCT07452562

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
Hesperidin (supplement), Placebo (supplement)
How long the study runs
Study runs about 12 months (dates as stated)
About the drug or intervention
Hesperidin — supplement: 500 mg/day Hesperidin capsules for 12 weeks · Placebo — supplement: Matching maltodextrin capsules for 12 weeks.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
60
Started
2026-01-07
Last checked
2026-02

Plain English Summary

What is this study?

  • • Testing a new treatment for multiple sclerosis
  • • NA - 60 participants
  • • This study is a randomised, double-blind, placebo-controlled trial investigating the effects of Hesperidin supplementation on cognitive function, fatigue, and stress

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with multiple sclerosis

Where?

  • • Swansea - FHMLS, Nutrition Lab

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

About This Trial

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.

More detail

Multiple Sclerosis (MS) is a chronic autoimmune condition characterized by neuro-inflammation, oxidative stress, and demyelination, often resulting in debilitating fatigue and cognitive dysfunction. While disease-modifying therapies exist, there is a significant need for accessible, low-risk adjunct interventions to manage these daily symptoms. Hesperidin is a flavanone found primarily in citrus fruits (e.g., oranges, lemons). Preclinical research using Experimental Autoimmune Encephalomyelitis (EAE)-the standard animal model for MS-has demonstrated that hesperidin supplementation can reduce disease severity and incidence, likely due to its potent anti-inflammatory and antioxidant properties. However, there is a paucity of randomized controlled trials translating these findings to human MS populations. Study Design \& Methodology. This study is a remote, randomised, double-blind, placebo-controlled, parallel-group trial in adults with Multiple Sclerosis. Participants will be randomized to receive either 500mg/day of Hesperidin or a matching placebo for a duration of 12 weeks. Statistical Analysis Plan. Data will be analysed using linear mixed-effects models. For the primary outcome (MFIS total score) and each secondary outcome, change from baseline to week 12 will be compared between intervention and placebo using fixed effects for group, time (baseline, week 12), and the group × time interaction, with a participant-level random intercept. The treatment effect will be estimated from the group × time interaction. Exploratory analyses will test whether baseline habitual diet modifies the intervention effect by adding a diet × group × time interaction term, with habitual diet operationalised using FFQ-derived polyphenol intake (energy-adjusted) and the Dietary Inflammatory Index (DII). In addition, exploratory symptom network analyses will examine whether the pattern of associations among symptoms differs between groups and changes from baseline to week 12.

Multiple Sclerosis

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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 and over
  • Who can join: All genders

What the study is looking for

  • ✓Diagnosis of Multiple Sclerosis, Aged 18 years or older.

Who cannot take part

  • ✗Known food allergies, intolerances, or significant gastrointestinal (GI) problems, Participants under the age of 18...
See the full criteria
Inclusion Criteria: * Diagnosis of Multiple Sclerosis, Aged 18 years or older. Exclusion Criteria: * Known food allergies, intolerances, or significant gastrointestinal (GI) problems, Participants under the age of 18 years.

Where Is This Study? (1 UK site)

FHMLS, Nutrition Lab

Swansea SA2 8PP, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Hayley Young, PhD

Sponsor contact

CONTACT

+44 (0) 1792 295908 h.a.young@swansea.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-02