Hydrogenology
Source-linked study record

Hydrogen gas (XEN) inhalation ameliorates airway inflammation in asthma and COPD patients

Wang ST et al. · QJM. 2020;113(12):870–875.

HumanInhaled H₂Published 2020Source 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 asthma or chronic obstructive pulmonary disease

Intervention and dose

A hydrogen-containing steam/air mixture inhaled once for 45 minutes · The generator initially produced 67% H₂/33% O₂, but an oxygen-adsorption cartridge removed O₂ before inhalation. Device gas was about 2.4% H₂ and nasal-cannula concentration about 0.1–0.3%.

Duration

One 45-minute inhalation session

Reported result

Some cytokines decreased, others did not, and one marker increased. No symptom, lung-function or longer-term clinical outcome was tested.

Main limitation

Acute uncontrolled study with 10 people per condition and many biomarkers. It cannot establish clinical benefit. Chinese public programs funded the study; authors declared no conflict.

Evidence and classification

What kind of evidence is this?

Evidence type

Human

Reported design

Prospective uncontrolled before-and-after study

Research topic

Respiratory health

Administration form

Inhaled H₂

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 asthma or chronic obstructive pulmonary disease

Sample

20 participants: asthma n=10, COPD n=10

Duration

One 45-minute inhalation session

Intervention

A hydrogen-containing steam/air mixture inhaled once for 45 minutes

Hydrogen form

H₂ in steam/air after device oxygen removal — not Brown’s gas at the point of delivery.

Dose or H₂ specification

The generator initially produced 67% H₂/33% O₂, but an oxygen-adsorption cartridge removed O₂ before inhalation. Device gas was about 2.4% H₂ and nasal-cannula concentration about 0.1–0.3%.

H₂ flow

Not reported. Total outlet flow was not provided, so H₂ flow in mL/min cannot be calculated.

O₂ delivered with H₂

O₂ was generated upstream but reportedly removed by a cartridge before inhalation; delivered O₂ flow was not reported.

Comparator

No concurrent comparator

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Blood and exhaled-breath-condensate cytokines

Reported result

Some cytokines decreased, others did not, and one marker increased. No symptom, lung-function or longer-term clinical outcome was tested.

Extraction completeness

Gas pathway, concentration, main biomarker results, funding and conflict statement checked in the free full text; flow remains unreported.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

Acute uncontrolled study with 10 people per condition and many biomarkers. It cannot establish clinical benefit. Chinese public programs funded the study; authors declared no conflict.

Applies directly to

Adults with asthma or COPD under a single short inhalation protocol.

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: 32407476 · DOI: 10.1093/qjmed/hcaa164

Publisher access

Open-access article.

Extraction basis

Free full text on PMC and Oxford Academic; identifiers cross-checked in PubMed.

Last reviewed

10 August 2026

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