Twice-Daily Oral Zinc in the Treatment of Patients With Coronavirus Disease 2019: A Randomized Double-Blind Controlled Trial

Zinc supplementation has been considered a potential therapy for coronavirus disease 2019 (COVID-19). We aimed to examine zinc efficacy in adult patients with COVID-19 infection. We conducted a prospective, randomized, double-blind, placebo-controlled multicenter trial. Patients who were tested posi...

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Veröffentlicht in:Clinical infectious diseases 2023-01, Vol.76 (2), p.185-191
Hauptverfasser: Ben Abdallah, Saoussen, Mhalla, Yosra, Trabelsi, Imen, Sekma, Adel, Youssef, Rim, Bel Haj Ali, Khaoula, Ben Soltane, Houda, Yacoubi, Hajer, Msolli, Mohamed Amine, Stambouli, Nejla, Beltaief, Kaouthar, Grissa, Mohamed Habib, Khrouf, Meriem, Mezgar, Zied, Loussaief, Chawki, Bouida, Wahid, Razgallah, Rabie, Hezbri, Karima, Belguith, Asma, Belkacem, Naouel, Dridi, Zohra, Boubaker, Hamdi, Boukef, Riadh, Nouira, Semir
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Sprache:eng
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Zusammenfassung:Zinc supplementation has been considered a potential therapy for coronavirus disease 2019 (COVID-19). We aimed to examine zinc efficacy in adult patients with COVID-19 infection. We conducted a prospective, randomized, double-blind, placebo-controlled multicenter trial. Patients who were tested positive for COVID-19 without end-organ failure were randomized to oral zinc (n = 231) or matching placebo (n = 239) for 15 days. The primary combined outcome was death due to COVID-19 or intensive care unit (ICU) admission ≤30 days after randomization. Secondary outcomes included length of hospital stay for inpatients and duration of COVID-19 symptoms with COVID-19-related hospitalization for outpatients. 190 patients (40.4%) were ambulatory and 280 patients (59.6%) were hospitalized. Mortality at 30 days was 6.5% in the zinc group and 9.2% in the placebo group (OR: .68; 95% CI .34-1.35); ICU admission rates were, respectively, 5.2% and 11.3% (OR: .43; 95% CI .21-.87). Combined outcome was lower in the zinc group versus the placebo group (OR: .58; 95% CI .33-.99). Consistent results were observed in prespecified subgroups of patients aged
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciac807