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									<identifier>oai:www.peertechzpublications.org:10.17352/jgro.000085</identifier>
									<datestamp>2020-06-10</datestamp>
									<setSpec>PTZ.JGRO:VOL6</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Novel therapy for COVID-19 does intravenous ozonated-saline affect blood and tissue oxygenation?
										</dc:title><dc:creator>Thorp JA</dc:creator><dc:creator> Hollonbeck SA</dc:creator><dc:creator> Viglione DD</dc:creator><dc:creator> Green PC</dc:creator><dc:creator> Hodge JR</dc:creator><dc:creator> Tamburro JA</dc:creator><dc:creator> Tran TN</dc:creator><dc:creator>Glassman DS</dc:creator><dc:description>&lt;p&gt;Introduction: Adjunctive ozone therapy for COVID-19 is being used successfully in China, Spain, Italy, and South America. One proposed mechanism is by improving blood / tissue oxygenation thus averting multiorgan system failure due to hypoxia. The purpose of this study was to determine if ozonated-saline administered intravenously affects the oxygenation and duration of time spent in a hypoxia chamber.&lt;/p&gt;&lt;br&gt;&lt;p&gt;Materials and methods: This was a prospective pilot study that used one volunteer who underwent seven experiments. Each included two runs in a hypoxia chamber that resulted in symptomatic oxygen desaturation. One subject was used as his own control in the hypoxia chamber before and after infusion of intravenous ozonated-saline in four paired experiments.Another 3 experiments were performed identically except ozone was not administered. The primary outcome was to test the null hypothesis that ozonated-saline infusion does not affect oxygenation.&lt;/p&gt;&lt;br&gt;&lt;p&gt;Results: In four experiments, ozone was associated with a significant increase in time the subject could remain in the hypoxia chamber (P&amp;lt; 0.05). In three control experiments without ozone, there was a significant decrease in time in the hypoxia chamber in the second run compared to the first (P &amp;lt;0.001). Compared to the first run there was a 32.4% increase in the proportion of time in the second run (after ozone) compared to the first run (P &amp;lt;0.0001). In contrast, in the three control experiments without ozone, there was significant decrease in proportion of time the subject could remain in the hypoxia chamber with an average decrease of -43.1% (P &amp;lt; 0.0001). Ozone therapy was associated with a significant delay in lowest oxygen desaturation (P &amp;lt;0.05). In contrast, in the three experimental runs without ozone there was a significant reduction in time to reach the nadir of the desaturation curve in the second run compared to that of the first (P &amp;lt; 0.05).&lt;/p&gt;&lt;br&gt;&lt;p&gt;Conclusions: Infusion of intravenous ozonated-saline significantly increases the duration of time that a subject can remain in hypoxia and delays the nadir of the oxygen de-saturation curve.&lt;/p&gt;</dc:description>
										<dc:publisher>Journal of Gynecological Research and Obstetrics - Peertechz Publications</dc:publisher>
										<dc:date>2020-06-10</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/jgro.000085</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Thorp JA et al.</dc:rights>
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