Boston Children's Hospital
Boston, Massachusetts, 02115, United States
NCT Number: NCT04046211
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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Notify Me18 year–35 year
All sexes
Interventional
Phase 1
Boston, Massachusetts, 02115, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Gas exposure for 24, 48 or 72 hours via high flow nasal cannula.
Time frame: During inhalation exposure
Any adverse effects will be codified according the the NCI CTCAE v5.0
Time frame: 2 hours following end of exposure period
Any adverse effects will be codified according the the NCI CTCAE v5.0
Time frame: 24 hours following end of exposure period
Any adverse effects will be codified according the the NCI CTCAE v5.0
Time frame: 5 days following end of exposure period
Any adverse effects will be codified according the the NCI CTCAE v5.0
Time frame: 1 hour before end of exposure period
Numerical change in mini mental state exam
Time frame: 1 hour before end of exposure period
FEV1
Time frame: 1 hour before end of exposure period
Forced vital capacity
Boston Children's Hospital
Other
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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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