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Recruiting NCT07452562

NCT07452562 Hesperidin RCT in MS

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Clinical Trial Summary
NCT ID NCT07452562
Status Recruiting
Phase
Sponsor Swansea University
Condition Multiple Sclerosis
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2026-01-07
Primary Completion 2027-01-18

Trial Parameters

Condition Multiple Sclerosis
Sponsor Swansea University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2026-01-07
Completion 2027-01-18
Interventions
HesperidinPlacebo

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Brief Summary

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.

Eligibility 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.

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