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A randomized controlled study of atomized inhalation of plasma-activated water in the treatment of progressive pneumonia that anti-COVID-19 drugs failured

A randomized controlled study of atomized inhalation of plasma-activated water in the treatment of progressive pneumonia that anti-COVID-19 drugs failured

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078706
Enrollment
Unknown
Registered
2023-12-15
Start date
2023-01-05
Completion date
Unknown
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19

Interventions

Sponsors

The First Affiliated Hospital of Air Force Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.18-85 years old (including 18 and 85 years old), regardless of gender. 2.The subjects tested positive for SARS-CoV-2 nucleic acid in sputum / nasal swabs / pharyngeal swabs / lower respiratory tract secretions before hospitalization, or positive for throat swab antigens during COVID-19 epidemic. Diagnosed with novel coronavirus infection. 3. The patient meets the diagnostic criteria of common(moderate) COVID-19 in the latest version of COVID-19 Diagnosis and Treatment Plan (9th Edition) issued by the China Health Commission. 4. After three to seven days of oral treatment with azivudine or nimatevir/ritonavir, the chest CT showed that the lesions of pneumonia increased or enlarged. 5. There is at least one possible risk factor for severe / critical disease: (1) age > 60 years old; (2) basic diseases such as cardio-cerebrovascular disease (including hypertension), chronic pulmonary disease (chronic obstructive pulmonary disease), diabetes, chronic liver disease, chronic kidney disease, tumor, etc. (3) immune deficiency (such as AIDS patients, decreased immune function caused by long-term use of corticosteroids or other immunosuppressive drugs); (4) obesity (body mass index = 30kg/m^2); (5) heavy smokers; (6) those who have not been vaccinated with new crown vaccine. 6. Understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe COVID-19 patients meet any of the following criteria:(1) shortness of breath, respiratory rate =30/min;(2) in resting state, oxygen saturation (SpO2) = 93% when inhaling air;(3) arterial oxygen partial pressure PaO2/ inhaled oxygen concentration (FiO2) = 300mmHg;(4) the clinical symptoms worsened progressively, and pulmonary imaging showed that the lesion progressed more than 50% within 24-48 hours. 2.Critical COVID-19 patients meet any of the following criteria:(1) respiratory failure and need mechanical ventilation;(2) shock;(3) ICU monitoring and treatment for patients with other organ failure. 3. Hyperallergenic constitution, including allergic bronchial asthma, etc. 4. Suspected or confirmed presence of bacteria, fungi, atypical pathogens and other pathogens in the lungs. 5. Pregnant or lactating women or those with positive pregnancy test, or those who plan to conceive within half a year. 6. The researchers believe that other factors that are not suitable for entering the trial, such as difficulties in communication, severe neurological and mental disorders, and severe physical weakness.

Design outcomes

Primary

MeasureTime frame
Improvement rate of chest imaging on the 5th day;

Secondary

MeasureTime frame
The rate of negative SARS-CoV-2 nucleic acid test;Quantitative score of symptoms (shortness of breath, cough, expectoration), signs;Oxygenation index, inflammatory factors, blood routine;The rate of common(moderate) COVID-19 aggravating to severe COVID-19;

Countries

China

Contacts

Public ContactLiqiang Song

The First Affiliated Hospital of the Air Force Military Medical University

songlq@fmmu.edu.cn+86 139 9116 0546

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026