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CORonavirus-19 mild to moderate pneumonia Management with blood Ozonization in patients with Respiratory failure (CORMOR) multicentric prospective randomized clinical trial.
Sozio, Emanuela; De Monte, Amato; Sermann, Giovanni; Bassi, Flavio; Sacchet, Davide; Sbrana, Francesco; Ripoli, Andrea; Curcio, Francesco; Fabris, Martina; Marengo, Stefania; Italiani, Daniele; Luciana Boccalatte-Rosa, Daniela; Tascini, Carlo.
  • Sozio E; U.O. Malattie Infettive, Dipartimento di Medicina dell'Università di Udine, Università di Udine e Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy. Electronic address: emanuela.sozio@gmail.com.
  • De Monte A; SOC Anestesia e Rianimazione 1, Università di Udine e Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy. Electronic address: amato.demonte@asufc.sanita.fvg.it.
  • Sermann G; SOC Anestesia e Rianimazione 1, Università di Udine e Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy. Electronic address: giovanni.sermann@asufc.sanita.fvg.it.
  • Bassi F; SOC Anestesia e Rianimazione 2, Università di Udine e Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy. Electronic address: flavio.bassi@asufc.sanita.fvg.it.
  • Sacchet D; U.O. Malattie Infettive, Dipartimento di Medicina dell'Università di Udine, Università di Udine e Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy. Electronic address: sacchet.davide@spes.uniud.it.
  • Sbrana F; U.O. Lipoapheresis and Center for Inherited Dyslipidemias, Fondazione Toscana Gabriele Monastrio, Via Moruzzi1, Pisa, Italy. Electronic address: francesco.sbrana@ftgm.it.
  • Ripoli A; Deep Health Unit, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy. Electronic address: ripoli@ftgm.it.
  • Curcio F; Istituto di Patologia Clinica, Azienda Sanitaria Universitaria Integrata di Udine (ASUID), Udine, Italy. Electronic address: francesco.curcio@asufc.sanita.fvg.it.
  • Fabris M; Istituto di Patologia Clinica, Azienda Sanitaria Universitaria Integrata di Udine (ASUID), Udine, Italy. Electronic address: martina.fabris@asufc.sanita.fvg.it.
  • Marengo S; SC di Medicina Interna e Unità di Terapia Semi Intensiva Internistica, Ordine Mauriziano di Torino, Torino, Italy. Electronic address: stefi.marengo@gmail.com.
  • Italiani D; Ospedale "Giuseppe Mazzini" Teramo, Teramo, Italy. Electronic address: danieleitaliani@outlook.it.
  • Luciana Boccalatte-Rosa D; UOC Anestesia e Rianimazione, Clinica Terapia Intensiva, PO San Luca Lucca Lucca, Italy. Electronic address: daliela.boccalatte-rosa@uslnordovest.toscana.it.
  • Tascini C; U.O. Malattie Infettive, Dipartimento di Medicina dell'Università di Udine, Università di Udine e Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy. Electronic address: carlo.tascini@uniud.it.
Int Immunopharmacol ; 98: 107874, 2021 Sep.
Article in English | MEDLINE | ID: covidwho-1267706
ABSTRACT

BACKGROUND:

Following positive experience on the use of blood ozonation in SARS-CoV-2, the CORMOR randomized trial was designed to evaluate the adjuvant role of oxygen/ozone therapy in mild to moderate SARS-CoV-2 pneumonia.

METHODS:

The trial (ClinicalTrial.gov NCT04388514) was conducted in four different Italian centers (April-October 2020). Patients were treated according to best available standard of care (SoC) therapy, with or without O3-autohemotherapy (O3-AHT).

RESULTS:

A total of 92 patients were enrolled SoC + O3-AHT (48 patients) were compared to the SoC treatment (44 patients). The two groups differed in steroids therapy administration (72.7% in SoC arm vs. 50.0% in O3-AHT arm; p = 0.044). Steroid therapy was routinely started when it was subsequently deemed as effective for the treatment of COVID-19 disease. No significant differences in mortality rates, length of hospital stay, mechanical ventilation requirement and ICU admission were observed. Clinical improvement in patients with pneumonia was assessed according to a specifically designed score (decrease in SIMEU class, improvement in radiology imaging, improvement in PaO2/FiO2, reduction in LDH and requirement of oxygen therapy ≤ 5 days). Score assessment was performed on day-3 (T3) and day-7 (TEnd) of O3-AHT treatment. A significant increase in the score was reported at TEnd, in the O3-AHT treatment arm (0 [0-1] in the SoC arm vs. 2 [1-3] the O3-AHT arm; p = 0.018). No adverse events related O3-AHT treatment was observed.

CONCLUSION:

In mild-to-moderate pneumonia due to SARS-CoV-2, adjuvant oxygen/ozone therapy did not show any effect on mortality, or mechanical intubation but show a clinical improvement a day 7 from randomization in a composite clinical endpoint. Larger Randomized prospective studies alone or in combination with steroids are needed to confirm our results.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ozone / Respiratory Insufficiency / COVID-19 / Lung Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Int Immunopharmacol Journal subject: Allergy and Immunology / Pharmacology Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ozone / Respiratory Insufficiency / COVID-19 / Lung Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: Int Immunopharmacol Journal subject: Allergy and Immunology / Pharmacology Year: 2021 Document Type: Article