Hydrogenology
Source-linked study record

Efficacy and Safety of Hydrogen Therapy in Patients with Early-Stage Interstitial Lung Disease

Tang C et al. · Ther Clin Risk Manag. 2023;19:1051–1061.

HumanH₂-rich waterPublished 2023Source checked
Study record, not medical adviceThis record reports what the source states. It is not medical advice and does not establish that molecular hydrogen is effective, safe or appropriate for any person.
Quick summary

Study at a glance

Evidence type

Human

Population or model

Adults with early-stage interstitial lung disease

Intervention and dose

350 mL hydrogen-rich water twice daily · 1.6 ppm dissolved H₂.

Duration

48 weeks

Reported result

The article reports more HRCT improvement and favorable CPI and DLCO-sb changes with H₂ water. FVC, FEV₁, FEV₁/FVC and TLC changes did not significantly differ; the primary endpoint was not significant in the full analysis set.

Main limitation

Single-center active-control trial without placebo water, 12 non-completers, imaging interpretation and mixed full-analysis/per-protocol findings. The water supplier provided H₂ water; public funding was reported.

Evidence and classification

What kind of evidence is this?

Evidence type

Human

Reported design

Single-center randomized parallel-group active-controlled trial

Research topic

Respiratory health

Administration form

H₂-rich water

Information not yet classified

Some editorial classification fields are still pending. The source-reported outcomes and result are shown below; Hydrogenology does not infer a positive or negative signal from prose automatically.

Reported in the source

Methods

Population or model

Adults with early-stage interstitial lung disease

Sample

87 randomized: H₂ water n=44; N-acetylcysteine n=43; 75 completed

Duration

48 weeks

Intervention

350 mL hydrogen-rich water twice daily

Hydrogen form

H₂ dissolved in water — H₂ only, not Brown’s gas and not inhalation.

Dose or H₂ specification

1.6 ppm dissolved H₂.

Comparator

N-acetylcysteine 600 mg orally three times daily

Reported, not endorsed

Outcomes and reported result

Outcomes measured

HRCT change, composite physiologic index, pulmonary-function measures and adverse events

Reported result

The article reports more HRCT improvement and favorable CPI and DLCO-sb changes with H₂ water. FVC, FEV₁, FEV₁/FVC and TLC changes did not significantly differ; the primary endpoint was not significant in the full analysis set.

Extraction completeness

Dose, full methods, results, funding and conflicts checked in open-access full text; independent appraisal remains incomplete.

A reported association, difference or mechanism is not automatically a clinical benefit.

Interpretation limits

Limitations and applicability

Main methodological cautions

Single-center active-control trial without placebo water, 12 non-completers, imaging interpretation and mixed full-analysis/per-protocol findings. The water supplier provided H₂ water; public funding was reported.

Applies directly to

Adults with early-stage ILD meeting the study criteria; not advanced fibrotic lung disease.

No single-study GRADE certainty rating is assigned. Read how records and evidence assessments are prepared.

Sources and status

Sources and record status

Identifiers

PMID: 38107500 · DOI: 10.2147/TCRM.S438044

Publisher access

Open-access full text is available through PMC and the publisher.

Extraction basis

Open-access PMC and publisher full texts plus PubMed record.

Last reviewed

10 August 2026

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