Intranasal Xylitol for the Treatment of COVID-19 in the Outpatient Setting: A Pilot Study

Autor: Evangelina, Soler, Amanda, de Mendoza, Víctor I, Cuello, Maria G, Silva-Vetri, Zoilangel H, Núñez, Ramsés G, Ortega, Syed A, Rizvi, Marcos, Sanchez-Gonzalez, Gustavo, Ferrer
Rok vydání: 2022
Předmět:
Zdroj: Cureus.
ISSN: 2168-8184
DOI: 10.7759/cureus.27182
Popis: It is well known that acute COVID-19 infection can present with a variety of symptoms, including fever, cough, rhinitis, loss of taste, and the cardinal sign of loss of smell (anosmia). Recently, nasal irrigations with saline and other agents have shown promise for the treatment of COVID-19. Xylitol has been shown to display virucidal effects against SARS-CoV-2. This study aimed to examine the efficacy of xylitol as an adjunct treatment for COVID-19 in an outpatient setting. In a randomized controlled double-blinded fashion, a total of 50 participants (F=30) consented to participate in this study. It was a population of 18 to 65 years of age, with polymerase chain reaction confirmed for SARS-COV-2 by nasopharyngeal swab, less than three days from the start of symptoms. This study's primary endpoint was time to clinical recovery, defined as the change from baseline to end of treatment in COVID-19 symptoms. Outcome variables were the changes in visual analog scale (VAS) and daily symptoms score (DSS) on Days 1-7, 14, and 28 after the initiation of the 14-day treatment. There were no differences between the treatment groups in any demographic and subject characteristics-related variables, including vaccination status. None of the patients were hospitalized, or required emergency visits in addition to no adverse reactions were reported. There were no statistically significant interactions found for VAS (P=0.124), DSS (P=0.448), and sense of smell (P=0.667). The proportion of patients reporting nasal congestion was higher (X
Databáze: OpenAIRE