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NCT07009691 · ClinicalTrials.gov registry record · NA
Hydrogen Water Intervention With Heart Rate Variability as an Outcome Biomarker in ME/CFS
A NA study of Chronic Fatigue Syndrome, sponsored by Stony Brook University.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT07009691 is a NA study of Chronic Fatigue Syndrome that is actively recruiting participants, run by Stony Brook University. The registered enrollment target is 50 participants, below the 7,244-participant average among 14 other Chronic Fatigue Syndrome trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07009691, a NA study of Chronic Fatigue Syndrome, is actively recruiting participants, sponsored by Stony Brook University.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to learn if the OTC supplement, hydrogen water, works to treat the fatigue-related symptoms and functional limitations in adults with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). It will also examine if heart rate variability (HRV) can be used to predict who will benefit from the hydrogen water treatment. The main questions it aims to answer are: Does the OTC supplement, hydrogen water, work to reduce the fatigue-related symptoms and improve functioning in participants who have ME/CFS? Can HRV be used to predict who will benefit from treatment with hydrogen water?
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Hydrogen water which is prepared from an OTC supplement.
Study Locations (1)
New York
- Stony Brook University - Stony Brook
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2025-06-09 |
| Est. Completion | 2026-05-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07009691
The ClinicalTrials.gov registry entry for NCT07009691 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 7,244-participant average among 14 other Chronic Fatigue Syndrome trials with a reported enrollment target (99% lower). The listed sponsor is Stony Brook University, which has 127 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Chronic Fatigue Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Hydrogen water which is prepared from an OTC supplement. is the first listed.
NCT07009691 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT07009691 about?
NCT07009691 is a clinical study titled "Hydrogen Water Intervention With Heart Rate Variability as an Outcome Biomarker in ME/CFS". The goal of this clinical trial is to learn if the OTC supplement, hydrogen water, works to treat the fatigue-related symptoms and functional limitations in adults with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). It will also examine if heart rate variability (HRV) can be used to pr...
What is the current status of trial NCT07009691?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2025-06-09. Estimated completion is 2026-05-31.
What conditions does trial NCT07009691 study?
This clinical trial studies the following conditions: Chronic Fatigue Syndrome.
What interventions are being tested in trial NCT07009691?
The interventions under investigation include: Hydrogen water which is prepared from an OTC supplement. (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT07009691?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07009691 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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