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Ozone Autohemotherapy in Covid19

Investigation the effects medical Ozone Autohemotherapy on clinical and para clinical features of patients with Covid19

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190618043923N4
Enrollment
20
Registered
2020-05-04
Start date
2020-04-25
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Coronavirus infection. Coronavirus infection, unspecified

Interventions

Intervention 1: Intervention group: Major Autohemotherapy with common treatments. 100 ml of the patient heparinized blood is mixed with 100 ml of ozone at a concentration of 30micro /mL O2-O3 and inje

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: 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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDawood Aghamohammadi

Tabriz University of Medical Sciences

daghamohamadi@yahoo.com+98 41 3336 1928

Outcome results

None listed

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