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Completed

NCT Number: NCT04046211

Safety of Inhaled Hydrogen Gas Mixtures in Healthy Volunteers

Hydrogen gas may decrease the degree or incidence of brain injury following ischemia. The purpose of this study is to determine the safety and tolerability of inhaled hydrogen gas at the dose exposures required for a clinical efficacy study in healthy adult participants. Participants will breathe a gas mixture that contains a low concentration of hydrogen gas in air through a high flow nasal cannula. Investigators will test for any changes in breathing and neurologic status, as well as lab tests during and following the exposure period.

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Key information

Conditions

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Boston Children's Hospital

Boston, Massachusetts, 02115, United States

About this study

Inhaled hydrogen gas (H2) has been shown to have significant protective effects on ischemic organs. Clinical trials abroad have shown promise that treatment of patients suffering from stroke, cardiac arrest, or heart attacks may benefit from inhaling hydrogen gas during the early recovery period.

The purpose of this study is to determine the safety and tolerability of inhaled hydrogen gas at the dose exposures required for a clinical efficacy study in healthy adult volunteers.

Study design. Eight (8) healthy adult participants will be recruited from the greater Boston area for this study. Consenting participants will be admitted to the hospital and will undergo a series of screens (questionnaires, examination, tests) to ensure suitability to participate. Eligible and consenting participants will then undergo exposure to 2.4% H2 in medical air via high flow nasal cannula for either 24 (n=2), 48 (n=2) or 72 (n=4) hours. Participants will be screened for adverse effects as follows: vital signs every 8 hours, nursing assessment of symptoms (codified based on the National Cancer Institute's Common Terminology Criteria for Adverse Events, CTCAE) every 8 hours, bedside spirometry daily, mini-mental state exam daily, physician physical exam daily, and serum testing (blood count, chemistry, liver and coagulation profile, venous blood gas) following exposure period.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 35
  • Able to remain inpatient for duration of admission (24-72 hours)

Exclusion criteria

  • History of any chronic illness, including respiratory disorders such as asthma, chronic obstructive pulmonary disease, prior acute lung injury or acute respiratory distress syndrome;
  • Inflammatory disorders, such as lupus erythematosus, inflammatory bowel disease;
  • Heritable disorders, such as trisomy 21, cystic fibrosis;
  • Mitochondrial disorders;
  • Currently smoking cigarettes or have a history of smoking cigarettes;
  • The regular use of prescription medications (except for contraceptive medications) within 30 days of enrollment;
  • Any lifetime inpatient hospitalization for respiratory illness;
  • Pregnancy.

Treatment and study plan

Hydrogen

Drug

Gas exposure for 24, 48 or 72 hours via high flow nasal cannula.

Primary outcomes

  1. Adverse effects/symptoms

    Time frame: During inhalation exposure

    Any adverse effects will be codified according the the NCI CTCAE v5.0

  2. Adverse effects/symptoms

    Time frame: 2 hours following end of exposure period

    Any adverse effects will be codified according the the NCI CTCAE v5.0

  3. Adverse effects/symptoms

    Time frame: 24 hours following end of exposure period

    Any adverse effects will be codified according the the NCI CTCAE v5.0

  4. Adverse effects/symptoms

    Time frame: 5 days following end of exposure period

    Any adverse effects will be codified according the the NCI CTCAE v5.0

Secondary outcomes

  1. Change in mini-mental state exam

    Time frame: 1 hour before end of exposure period

    Numerical change in mini mental state exam

  2. Bedside spirometry

    Time frame: 1 hour before end of exposure period

    FEV1

  3. Bedside spirometry

    Time frame: 1 hour before end of exposure period

    Forced vital capacity

Sponsors and collaborators

Lead sponsor

Boston Children's Hospital

Other

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Aug 6, 2019
Registry last updated
May 6, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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