Clinical improvement | Hospitalization | Inflammatory/thromboembolic/infectious/metabolic markers | Radiological aspects | Viral infection | Adverse events | |||||||||||||||||||||||||||||||
General improvement in clinicalsymptoms of COVID-19 | Improvement of cough | Reduction of body temperature | Improvement of shortness of breath | Improvement of respiratory function | Improvement of oxygen saturation | Early weaning from oxygen support | Reduction in the need for invasivemechanical ventilation | Faster recovery from acute respiratorydistress syndrome (ARDS) | Prevention of clinical worsening | Reduction of mortality | Reduction of hospital stay | Reduction in the need for admission tothe intensive care unit (ICU) | Decrease in C-reactive protein | Reduction of ferritin | Decreased lactate dehydrogenase | Decreased fibrinogen | Decrease in interleukin 6 | D-dimer decrease | Leukocyte normalization | Normalization of lymphocytes | Decrease in procalcitonin | Decreased Neutrophil-LymphocyteRatio | Normalization of alanineaminotransferase | Radiological improvement of lunglesions | Reduction of viral load | Faster RT-PCR negative | Presence | Absence | Unmentioned | |||||||
Study | Name | Country | Therapy | Type of study | Number of hospitalized patients who received Ozone Therapy | Pneumonia severity level | ||||||||||||||||||||||||||||||
A | Wu et al. (2020)* | China | GAHT, 40 mcg / ml, 100 ml, 1: 1, once a day on the first day and twice a day on the second to the fifth day, for 5 days, totaling 9 sessions | Report of a case | 1 | Severe | X | X | X¶ | X | X | X | X | X | X | X | X | |||||||||||||||||||
B | Zheng et al. (2020)* | China | GAHT, 20 mcg / ml, 100 ml, 1: 1, once a day for 7 days, totaling 7 sessions | Report of a case | 2 | Severe | X | X | X | X | X | X | X | X | ||||||||||||||||||||||
C | Franzini et al. (2020) | Italy | Clinical trial | 50 | Moderate | X | X | X | X | X | X | X | X | X | X | X | ||||||||||||||||||||
D | Hernández et al. (2020)* | Spain | GAHT, 40 mcg / ml, 200 ml, 1: 1, 2 timer a day, for 3 days, totaling 6 sessions | Report of a case | 3 | Severe | X | X | X | X | X | X | X | X | X | X | X | |||||||||||||||||||
E | Tascini et al. (2020) | Italy | GAHT, 40 mcg / ml, 200 ml, 1: 1, once a day, for 3 days, totaling 3 sessions | Cases and cortrols study | 30 | Mild to moderate | X | X | X | X | X | |||||||||||||||||||||||||
F | Hernández et al. (2021) | Spain | GAHT, 40 mcg / ml, 200 ml, 1: 1, 2 times a day for 5 days, totaling 10 sessions | Prospective case-control study | Severe | X | X | X | X | X | X | X | ||||||||||||||||||||||||
G | Fernández-Cuadros et al.(2020)* | Spain | IR, 35 mcg / ml, 100 ml, once a day for 5 to 10days, for a total of 5 to 10 sessions | Quasi-experimental prospective cohort study | Severe | X | X | X | X | X | X | X | X | XΔ | ||||||||||||||||||||||
H | Pena-Lora et al. (2020)* | Spain | IR, 35 mcg / ml, 100 ml, once a day for 5 days, totaling 5 sessions | Report of a case | 1 | Severe | X | X | X | X | X | X | X | X | X | X | X | |||||||||||||||||||
I | Shah et al. (2020) | India | 1st) IR, 40 mcg / mL, 150mL, 2 times a day for9 days, totaling 18 sessions 2nd) PAHT 25mcg /mL, 5mL of O3 and 2 to 3 ml of blood, once aday for 9 days, totaling 9 sessions | Randomized clinical trial | 30 | Mild to moderate | X | X | X | X | X | X | X¤ | X¤ | X¤ | X | X | |||||||||||||||||||
J | Razzaq et al. (2020)* | Iraq | SFO3, 35-45mcg / mL, 500mL, 3 to 5 minutes of preparation in continuous bubbling, infusion in15 minutes, 1 to 2 times a day, for 5-10 days. | Clinical trial | 104 | Moderate to severe | X | X | X | X | ||||||||||||||||||||||||||
K | Schwartz et al. (2020) | Spain | SFO3, 3-5mcg / mL, 200mL, 10 minutes of preparation in continuous bubbling, infusion of15 to 30 minutes, once a day, for 10 days. | Non-randomized clinical trial | 35 | Severe | X | X | X | X | X | X | X | X | X | X | X | X | X | |||||||||||||||||
J | Sharma et al. (2021) | India | SFO3. 5mcg / mL, 200mL, 20 minutes of preparation in continuous bubbling, infusion of 1hour, once a day, for 8 days. | Clinical trial | 10 | Moderate | X | X | X | X | X | X | X | X | X | X | X | X | X | XΦ | ||||||||||||||||
L | Hendawy et al. (2021) | Egypt | 1) IR, 12.6 mcg / mL, 2 liters, two sessions2) IR, 12.6mcg/mL, 2 liters, one session | Report of a case | 3 | Mild and severe | X | X | X | X | X | X | X | |||||||||||||||||||||||
Total Results | 13 | 2 | 3 | 2 | 6 | 6 | 2 | 3 | 2 | 4 | 2 | 6 | 2 | 10 | 7 | 8 | 2 | 6 | 8 | 1 | 2 | 1 | 1 | 1 | 7 | 1 | 1 | 3 | 6 | 4 |
Note: * Studies without statistics; Δ Discreet weather, gas sensation; . Epistaxis associated with the use of heparin; ¤ Falling of inflammatory markers, without significant statistics; ¶ Improvement of refractory hypoxemia; Φ Mild pain at the injection site and headache.