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Clinical study of ozonated water enema in the improvement of COVID-19 patients

Clinical study of ozonated water enema in the improvement of COVID-19 patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068233
Enrollment
Unknown
Registered
2023-02-10
Start date
2023-02-11
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

COVID-19

Interventions

Ozonated water enema group:Ozonated water enema
Deionized water enema group:Deionized water enema

Sponsors

Department of Anesthesiology and Pain Mnagement, Shanghai East Hospital, School of Medicine, Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years old, male or female; 2. The diagnostic criteria for severe COVID-19 in adults according to the 2022 diagnosis and treatment Plan for COVID-19 (trial 9th edition) are as follows: (1) 2019-ncov nucleic acid test was positive; (2) Confirmed epidemiological history within 14 days; (3) Clinical manifestations related to COVID-19 such as fever and/or respiratory symptoms; (4) Chest CT has the imaging characteristics of COVID-19; (5) Anyone who meets any of the following: 1) Shortness of breath, RR >= 30 times/min; 2) In the resting state, oxygen saturation during air inhalation was 50%; (6) Critical type meets one of the following conditions: 1) respiratory failure requiring mechanical ventilation; 2) the onset of shock; 3) Complicated with other organ failure requiring ICU care; 3. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Massive blood loss, acute bleeding, anemia (Hb < 90 g/L); 2. Severe coagulopathy or thrombocytopenia less than 50 x 10^9/L; 3. Thalassemia, sickle cell anemia, glucose-6-phosphate dehydrogenase deficiency (patients with faba disease); 4. Toxic diffuse goiter (Graves' disease); 5. Severe unstable cardiovascular disease, acute myocardial infarction; 6. Women who are pregnant or lactating or menstruating; 7. Patients with mental illness, nervous system disease or high sensitivity; 8. Continuous use of immunosuppressants or organ transplantation within the past 6 months; 9. Investigator assessment of subjects unable or unwilling to comply with protocol requirements; 10. Intestinal obstruction, intestinal perforation, acute alcohol poisoning.

Design outcomes

Primary

MeasureTime frame
IL-6;

Secondary

MeasureTime frame
C-reactive protein;Procalcitonin;28-day survival rate;IL-8;IL-1ß;stool for routine;TNF-a;oxygenation index;Sequential Organ Failure Assessment Score;

Countries

China

Contacts

Public ContactLijun Liao

Department of Anesthesiology and Pain Mnagement, Shanghai East Hospital, School of Medicine, Tongji University

lliao@tongue.edu.cn+86 138 1742 8913

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026