Evidence map›Paper›PMID 36039203›Full record

ArticleCureus2022

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

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

Open access · diamondAbstract read
In one paragraph

Article in Cureus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Evangelina SolerDepartment of Pulmonolgy, Clinica Corazones Unidos, Santo Domingo, DOM.
Amanda de MendozaDepartment of Pulmonolgy, Clinica Corazones Unidos, Santo Domingo, DOM.
Víctor I CuelloDepartment of Pulmonolgy, Clinica Corazones Unidos, Santo Domingo, DOM.
Maria G Silva-VetriDepartment of Research, Universidad Nacional Pedro Henríquez Ureña School of Medicine, Santo Domingo, DOM.
Zoilangel H NúñezDepartment of Research, Universidad Nacional Pedro Henríquez Ureña School of Medicine, Santo Domingo, DOM.
Ramsés G OrtegaDepartment of Research, Universidad Nacional Pedro Henríquez Ureña School of Medicine, Santo Domingo, DOM.
Syed A RizviGraduate Medical Education and Biomedical Sciences, Larkin Hospital and University, Miami, USA.
Marcos Sanchez-GonzalezGraduate Medical Education, Larkin Community Hospital, South Miami, USA.
Gustavo FerrerPulmonary Critical Care, Aventura Hospital and Medical Center, Aventura, USA.
Aventura Hospital and Medical Center · USUniversidad Nacional Pedro Henríquez Ureña · DOLarkin University · USUniversidad Interamericana · DO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

Indexed as

anosmiacovid-19intranasal therapiesnasal hygienesalinesars-cov-2xylitol

Identifiers

PMID36039203
PMCPMC9395150
OpenAlexW4286770911

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.