COVID-19 Clinical Trial
Official title:
A Multi-center, Randomized, Parallel-Controlled Clinical Trial of the Application of A Hydrogen-Oxygen Generator With Nebulizer in the Improvement of Symptoms in Patients Infected With COVID-19
This study will evaluate the efficacy and safety of Hydrogen-Oxygen Generator with Nebulizer (model AMS-H-03) developed by Shanghai Asclepius Meditech Co., Ltd. as an adjuvant therapy for the patients with COVID-19 infected pneumonia in improving the clinical symptoms and reducing the incidence of severe pneumonia, as compared with the reference device of EverFlo Oxygen Concentrator (registration certificate No.: NMPA Registration Standard: 20162542389) manufactured by Respironics, Inc. US.
A multi-center, randomized, parallel-controlled clinical trial design is used in this study.
Eligible subjects will be randomized into the study group and control group in a 1:1 ratio.
In addition to the supportive treatments depending on the condition, the subjects in the
study group will inhale the mixed gas of hydrogen/oxygen (hydrogen concentration 66%, oxygen
concentration 33%) at a flow rate of 6 L/min every day using the Hydrogen/Oxygen Generator
with Nebulizer (model AMS-H-03) developed by Shanghai Asclepius Meditech Co., Ltd. during the
treatment, with the total use of no less than 6 hours per day, and the other combination
treatments will be decided by the investigator depending on the clinical needs; the subjects
in the control group will inhale the gas at a flow rate of 2 L/min every day using the
reference device of EverFlo Oxygen Concentrator (registration certificate No.: NMPA
Registration Standard: 20162542389) developed by Respironics, Inc. US. during the treatment,
with the total use of no less than 6 hours per day, and the other combination treatments will
be decided by the investigator depending on the clinical needs. During the treatment, the
peripheral blood oxygen saturation should be monitored and the oxygen concentration should be
increased when necessary (the peripheral oxygen saturation is less than 95% for 30 seconds
and other causes have been excluded). Oxygen may be supplied by other devices if the oxygen
concentration is sufficient for the subjects in the study group. The oxygen saturation and
respiratory rate will be measured at the resting state every day during the treatment, namely
after the end of daily treatment and 30 minutes after the inhalation of oxygen and
hydrogen/oxygen.
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