Could breathing hydrogen protect the aging brain?
NCT ID NCT07757542
First seen Aug 11, 2026 · Last updated Aug 12, 2026 · Updated 1 time
Summary
This study tests whether inhaling a low concentration of hydrogen gas each day is safe and might help people with mild cognitive impairment. Participants, aged 50 to 80, will breathe in 4% hydrogen for one hour daily over 12 weeks, followed by 12 weeks without it. Researchers will monitor for side effects and use memory and naming tests to see if cognitive function changes. The goal is to gather initial safety data and see if this approach warrants larger studies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Molecular hydrogen gas administered by inhalation
- What this could lead to
- If safe and effective, daily hydrogen inhalation could offer a simple, non-drug way to help preserve memory and thinking in people with mild cognitive impairment.
- What could go wrong
- This is a small pilot study, not designed to prove effectiveness. It focuses on safety and feasibility, and results may not generalize. The therapy's benefits are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 34 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients diagnosed with mild cognitive impairment (MCI) with an overall good health condition * generally good health, with the ability to perform daily activities independently (modified Rankin score 0-2, Barthel index minimum 70 points) * age between 50 and 80 years, ensuring inclusion of individuals within the typical risk range for cognitive decline * a reliable study partner or caregiver who can provide accurate information about the participant's cognitive and functional abilities throughout the study * stable medical condition, without major fluctuations in health status that could interfere with cognitive assessments * signed informed consent, ensuring that participants understand the study protocol and potential risks Exclusion Criteria: * pregnancy or lactation, as the safety of hydrogen inhalation therapy in these populations has not been established * use of medications or investigational treatments that could significantly affect cognitive function or interfere with study outcomes * history of severe psychiatric disorders such as major depression, bipolar disorder, or schizophrenia, which may independently influence cognitive performance * history of cerebrovascular events, including recent stroke or transient ischemic attack, which may confound cognitive outcomes * severe cardiovascular diseases, including uncontrolled hypertension, recent myocardial infarction, or heart failure, that could pose additional risks during the study * chronic kidney disease (stage 3 or higher), as impaired renal function may alter systemic metabolism and affect the study's findings * significant respiratory disorders, such as severe chronic obstructive pulmonary disease (COPD) or restrictive lung diseases, that could impact the safety of hydrogen inhalation * known hypersensitivity or allergic reactions to materials used in the hydrogen delivery system, such as nasal cannulas or facial masks * recent participation in another clinical trial within the past 90 days, to prevent potential interactions and ensure unbiased study results
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cerebrovaskularni poradna s.r.o.
RECRUITINGOstrava, Moravian-Silesian Region, 70200, Czechia
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