Hydrogenology
Hydrogenology editorial study record

Using oral molecular hydrogen supplements to combat microinflammation in humans: a pilot observational study

Lu KC, Shen MC, Wang RL, Chen WW, Chiu SH, Kao YH, Liu FC, Hsiao PJ. · International journal of medical sciences. 2024;21(12):2390-2401.

HumanH₂-rich waterPublished 2024
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Human

Reported design

Human interventional or observational study

Research topic

Oral and dental health

Administration classification

H₂-rich water

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Human participants studied for oral and dental health; aged 20 years. See eligibility criteria in the linked full text.

Sample

Human study; the full text reports 30 patients, with group/assay counts including n=10.

Duration

28 days

Intervention

Full text reports H₂ dissolved in drinking water plus an oral H₂-generating preparation. Detected intervention quantities or schedules: 200 ppb, 28 days, 4 weeks, 100%, 10 μm.

Hydrogen form

H₂ dissolved in drinking water plus an oral H₂-generating preparation — H₂ only unless the full text explicitly reports oxygen co-delivery.

H₂ specification

H₂-related quantities reported in the intervention passages: 200 ppb, 28 days, 4 weeks, 100%, 10 μm. Values are not combined across different experimental arms.

H₂ flow

Not applicable — no inhaled H₂ intervention was identified in the full article.

O₂ delivered with H₂

No inhaled O₂ co-delivery was identified for this non-inhalation intervention.

Comparator

Control or comparison condition reported in the full article; see the linked methods for arm-specific details.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

survival or mortality, clinical symptoms or functional scores, tumor growth or cancer markers, inflammation and cytokines, oxidative-stress and antioxidant markers, apoptosis or cell injury

Reported result

Article-reported result excerpt (24 words maximum): “Results: Compared to HRW and CaH_2, OSHCs demonstrated a prolonged reduction in ORP for 60 minutes in vitro and enabled a regulated release of…” This excerpt is not a complete result summary; consult the linked full text for all positive and null findings.

Results-extraction completeness

The complete machine-readable article was checked for source identity, methods, intervention quantities, results, tables, funding and conflict declarations. This public record is based on the full article.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Human evidence; design, sample size and comparator limit interpretation. Funding or grant information is reported in the full article. The article declares no conflicts of interest.

Applies directly to

Applies only to the population and protocol reported in this oral and dental health article.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 39310256 · DOI: 10.7150/ijms.101114

Publisher access

A free full article is available through PubMed Central.

Extraction basis

Official Europe PMC JATS full article and PubMed/PMC identifiers; structured full-text extraction and validation completed 8 August 2026.

Record revision

2026-08-10