Ozone Autohemotherapy in Covid19
- Conditions
- Coronavirus infection.Coronavirus infection, unspecifiedB34.2
- Registration Number
- IRCT20190618043923N4
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Being 20-60 years of age
Having a positive reverse-transcriptase polymerase chain reaction test for SARS-CoV-2
Being admitted to the intensive care unit
Receiving invasive mechanical ventilation that began a short time before admission or in the intensive care unit
Patients with an anticipated survival length of fewer than 24?hours
Patients with a body mass index of 35 kg/m2 and over
Patients with a history of blood disorders
Patients with a history of renal or liver failure or chronic obstructive pulmonary disease
Pregnant or lactating women
Patients who were joined in other clinical trials
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Complete Blood cell count and diffrential count. Timepoint: Complete Blood cell count and diffrential count at the beginning of the study (before the intervention) and 7, 14 and 21 days after the start of ozone autohemotherapy. Method of measurement: Biochemical analysis.;Liver function tests. Timepoint: Liver function tests at the beginning of the study (before the intervention) and 7, 14 and 21 days after the start of ozone autohemotherapy. Method of measurement: Biochemical analysis.;Renal function tests. Timepoint: Renal function tests at the beginning of the study (before the intervention) and 7, 14 and 21 days after the start of ozone autohemotherapy. Method of measurement: Biochemical analysis.
- Secondary Outcome Measures
Name Time Method Mechanical ventilator weaning time. Timepoint: Mechanical ventilator weaning time during the study after the start of ozone autohemotherapy. Method of measurement: Comment by the treating physician.