Skip to content

A multicenter randomized controlled trial for ozone autohemotherapy in the treatment of novel coronavirus pneumonia (COVID-19)

A multicenter randomized controlled trial for ozone autohemotherapy in the treatment of novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030102
Enrollment
Unknown
Registered
2020-02-23
Start date
2020-02-24
Completion date
Unknown
Last updated
2020-02-25

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

control group with common NCP:conventional treatment
experimental group with common NCP:conventional treatment combined with ozone therapy
experimental group with severe NCP:conventional treatment combined with ozone therapy
control group with severe NCP:conventional treatment
experimental group with critical NCP:conventional treatment combined with ozone therapy
control group with critical NCP:conventional treatment

Sponsors

Tianjin Huanhu Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years; 2. Within 1 week of onset; 3. Meet the diagnostic criteria of common, severe and critical NCP, according to "Pneumonitis Diagnosis and Treatment Scheme for Novel Coronavirus Pneumonia (Trial Version 6)". 4. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Any situation that does not allow the program to proceed safely; 2. The patient may be transferred to a non-participating hospital within 72 hours; 3. Those who have continued to use immunosuppressive agents or organ transplants for the past 6 months; 4. Glucose-6-phosphate dehydrogenation Enzyme deficiency (faba bean disease) 5; 5. Patients treated with any of the antiviral drugs listed in the protocol during hospitalization before enrollment; 6. Those participating in other clinical trials. 7. Those who are allergic to ozone or hypersensitive.

Design outcomes

Primary

MeasureTime frame
Chest imaging;RNA test of COVID-19;Time to remission/disappearance of primary symptoms: defined as the number of days when the three main symptoms of fever, cough, and shortness of breath are all relieved / disappeared;Completely antipyretic time: completely antipyretic was defined as the body temperature return to normal for over 24 hours.;Blood oxygen saturation;Time to 2019-nCoV RT-PCR negativity: defined as the last test time for two consecutive negative respiratory viral nucleic acid tests (sampling interval of at least 1 day);Liver, renal and heart function;

Secondary

MeasureTime frame
Conversion of severe cases: defined as the number of severe and critical cases that occurred after the study was included and the intervention was initiated;Incidence of medical complications during hospitalization: defined as medical complications during pneumonia isolation hospitalization due to novel coronavirus infection, including combined bacterial infections, exacerbation of underlying diseases, etc.;Routine blood test;C-reactive protein;Blood gas analysis;

Countries

China

Contacts

Public ContactXiaoguang Tong

Tianjin Huanhu Hospital

Tongxg@yahoo.com+86 13820088121

Outcome results

None listed

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