Chronic Fatigue Syndrome Clinical Trials

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Randomized Controlled Trial of Moderate Dose Hydrogen Water as a Treatment for ME/CFS

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a 16-week controlled treatment trial of an over-the -counter supplement, hydrogen water, for individuals with ME/CFS patients. An active treatment condition will be compared to a placebo-control condition. The study will also seek confirmation of heart rate variability (HRV) as a biomarker, that is, as a predictor of improvement vs. non-improvement to be assessed at treatment termination. The HRV biomarker hypothesis is based on a finding that High Frequency HRV (cardio-parasympathetic measure) biologically separated improvers and non-improvers in my previous ME/CFS observational study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Patients aged 18-65 of both sexes

• considered physically capable and willing to perform the study tasks

• Meet validated phone-screen eligibility for ME/CFS criteria

• Participant has internet and computer

Locations
United States
New York
Stony Brook University
RECRUITING
Stony Brook
Contact Information
Primary
Fred Friedberg, PhD
Fred.Friedberg@stonybrookmedicine.edu
16316381931
Time Frame
Start Date: 2026-08-15
Estimated Completion Date: 2027-07
Participants
Target number of participants: 80
Treatments
Placebo_comparator: Placebo condition
Magnesium tablet, 3 tablets a day dissolved in water, without active ingredient of molecular hydrogen. 16 week duration.
Experimental: Active hydrogen water intervention
Related Therapeutic Areas
Sponsors
Leads: Fred Friedberg

This content was sourced from clinicaltrials.gov