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Safety and effectiveness of high-dose vitamin C in patients with COVID-19: a randomized open-label clinical trial.

Identifieur interne : 000351 ( Main/Corpus ); précédent : 000350; suivant : 000352

Safety and effectiveness of high-dose vitamin C in patients with COVID-19: a randomized open-label clinical trial.

Auteurs : Saeidreza Jamalimoghadamsiahkali ; Besharat Zarezade ; Sogol Koolaji ; Seyedahmad Seyedalinaghi ; Abolfazl Zendehdel ; Mohammad Tabarestani ; Ehsan Sekhavati Moghadam ; Ladan Abbasian ; Seyed Ali Dehghan Manshadi ; Mohamadreza Salehi ; Malihe Hasannezhad ; Sara Ghaderkhani ; Mohsen Meidani ; Faeze Salahshour ; Fatemeh Jafari ; Navid Manafi ; Fereshteh Ghiasvand

Source :

RBID : pubmed:33573699

English descriptors

Abstract

BACKGROUND

Vitamin C is an essential water-soluble nutrient that functions as a key antioxidant and has been proven to be effective for boosting immunity. In this study, we aimed to assess the efficacy of adding high-dose intravenous vitamin C (HDIVC) to the regimens for patients with severe COVID-19 disease.

METHODS

An open-label, randomized, and controlled trial was conducted on patients with severe COVID-19 infection. The case and control treatment groups each consisted of 30 patients. The control group received lopinavir/ritonavir and hydroxychloroquine and the case group received HDIVC (6 g daily) added to the same regimen.

RESULTS

There were no statistically significant differences between two groups with respect to age and gender, laboratory results, and underlying diseases. The mean body temperature was significantly lower in the case group on the 3rd day of hospitalization (p = 0.001). Peripheral capillary oxygen saturations (SpO

CONCLUSIONS

We did not find significantly better outcomes in the group who were treated with HDIVC in addition to the main treatment regimen at discharge. Trial registration irct.ir (IRCT20200411047025N1), April 14, 2020.


DOI: 10.1186/s40001-021-00490-1
PubMed: 33573699
PubMed Central: PMC7877333

Links to Exploration step

pubmed:33573699

Le document en format XML

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<name sortKey="Dehghan Manshadi, Seyed Ali" sort="Dehghan Manshadi, Seyed Ali" uniqKey="Dehghan Manshadi S" first="Seyed Ali" last="Dehghan Manshadi">Seyed Ali Dehghan Manshadi</name>
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<nlm:affiliation>Department of Infectious Diseases, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</nlm:affiliation>
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<name sortKey="Ghaderkhani, Sara" sort="Ghaderkhani, Sara" uniqKey="Ghaderkhani S" first="Sara" last="Ghaderkhani">Sara Ghaderkhani</name>
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<nlm:affiliation>Department of Infectious Diseases, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</nlm:affiliation>
</affiliation>
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<name sortKey="Meidani, Mohsen" sort="Meidani, Mohsen" uniqKey="Meidani M" first="Mohsen" last="Meidani">Mohsen Meidani</name>
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<name sortKey="Manafi, Navid" sort="Manafi, Navid" uniqKey="Manafi N" first="Navid" last="Manafi">Navid Manafi</name>
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<nlm:affiliation>Max Rady College of Medicine, University of Manitoba, Winnipeg, Canada.</nlm:affiliation>
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<name sortKey="Ghiasvand, Fereshteh" sort="Ghiasvand, Fereshteh" uniqKey="Ghiasvand F" first="Fereshteh" last="Ghiasvand">Fereshteh Ghiasvand</name>
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<term>Ascorbic Acid (administration & dosage)</term>
<term>Ascorbic Acid (therapeutic use)</term>
<term>Body Temperature (MeSH)</term>
<term>COVID-19 (drug therapy)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Hydroxychloroquine (therapeutic use)</term>
<term>Intensive Care Units (MeSH)</term>
<term>Length of Stay (MeSH)</term>
<term>Lopinavir (therapeutic use)</term>
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<term>Middle Aged (MeSH)</term>
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<term>Respiratory Distress Syndrome (virology)</term>
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<p>
<b>BACKGROUND</b>
</p>
<p>Vitamin C is an essential water-soluble nutrient that functions as a key antioxidant and has been proven to be effective for boosting immunity. In this study, we aimed to assess the efficacy of adding high-dose intravenous vitamin C (HDIVC) to the regimens for patients with severe COVID-19 disease.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>An open-label, randomized, and controlled trial was conducted on patients with severe COVID-19 infection. The case and control treatment groups each consisted of 30 patients. The control group received lopinavir/ritonavir and hydroxychloroquine and the case group received HDIVC (6 g daily) added to the same regimen.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>There were no statistically significant differences between two groups with respect to age and gender, laboratory results, and underlying diseases. The mean body temperature was significantly lower in the case group on the 3rd day of hospitalization (p = 0.001). Peripheral capillary oxygen saturations (SpO</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>We did not find significantly better outcomes in the group who were treated with HDIVC in addition to the main treatment regimen at discharge. Trial registration irct.ir (IRCT20200411047025N1), April 14, 2020.</p>
</div>
</front>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Vitamin C is an essential water-soluble nutrient that functions as a key antioxidant and has been proven to be effective for boosting immunity. In this study, we aimed to assess the efficacy of adding high-dose intravenous vitamin C (HDIVC) to the regimens for patients with severe COVID-19 disease.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">An open-label, randomized, and controlled trial was conducted on patients with severe COVID-19 infection. The case and control treatment groups each consisted of 30 patients. The control group received lopinavir/ritonavir and hydroxychloroquine and the case group received HDIVC (6 g daily) added to the same regimen.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">There were no statistically significant differences between two groups with respect to age and gender, laboratory results, and underlying diseases. The mean body temperature was significantly lower in the case group on the 3rd day of hospitalization (p = 0.001). Peripheral capillary oxygen saturations (SpO
<sub>2</sub>
) measured at the 3rd day of hospitalization was also higher in the case group receiving HDIVC (p = 0.014). The median length of hospitalization in the case group was significantly longer than the control group (8.5 days vs. 6.5 days) (p = 0.028). There was no significant difference in SpO
<sub>2</sub>
levels at discharge time, the length of intensive care unit (ICU) stay, and mortality between the two groups.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">We did not find significantly better outcomes in the group who were treated with HDIVC in addition to the main treatment regimen at discharge. Trial registration irct.ir (IRCT20200411047025N1), April 14, 2020.</AbstractText>
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<Affiliation>Department of Infectious Diseases, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.</Affiliation>
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