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Evaluation of Silver Nanoparticles for the Prevention of COVID-19

C

Cluster de Bioeconomia de Baja California, A.C

Status

Completed

Conditions

Coronavirus Disease 2019 (COVID-19)

Treatments

Device: Mouthwash and nose rinse with the AgNPs solution
Device: Mouthwashes and nose rinse in a conventional way

Study type

Interventional

Funder types

Other

Identifiers

NCT04894409
CONBIOETICA-02-CEI-001-20170

Details and patient eligibility

About

In this research, silver nanoparticles (AgNPs) were tested in vitro and shown to have an inhibitory effect on SARS-CoV-2 infection in cultured cells. Subsequently, the investigators assessed the effects of mouthwash and nose rinse with ARGOVIT® silver nanoparticles (AgNPs), in the prevention of SARS-CoV-2 contagion in health workers consider as high-risk group of acquiring the infection in the General Tijuana Hospital, Mexico, a hospital for the exclusive recruitment of patients diagnosed with COVID-19.

Full description

SARS-CoV-2 infection in hospital areas is of a particular concern, since the close interaction between health care personnel and patients diagnosed with COVID-19, which allows virus to be easily spread between them and subsequently to their families and communities. Preventing SARS-CoV-2 infection among healthcare personnel is essential to reduce the frequency of infections and outbreaks during the pandemic. In a first step, silver nanoparticles (AgNPs) were tested in vitro to determine an inhibitory effect on SARS-CoV-2 infection in cultured cells. Subsequently, the investigators assess the effects of mouthwash and nose rinse with ARGOVIT® silver nanoparticles (AgNPs), in the prevention of SARS-CoV-2 contagion in health workers consider as high-risk group of acquiring the infection in the General Tijuana Hospital, Mexico, a hospital for the exclusive recruitment of patients diagnosed with COVID-19. The investigators present a prospective randomized study of 231 participants that was carried out for 9 weeks (during the declaration of a pandemic). The "experimental" group was instructed to do mouthwash and nose rinse with the AgNPs solution; the "control" group was instructed to do mouthwashes and nose rinse in a conventional way.

Enrollment

231 patients

Sex

All

Ages

20 to 73 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men and women health workers in the General Tijuana Hospital, Mexico who works in high-risk areas with direct contact with patients infected and diagnosed with COVID-19.

Exclusion criteria

  • persons with history of hypersensitivity to silver (rashes and other contraindications),
  • a history of SARS-CoV-2 infection in the three months prior to the start of the study, any respiratory distress,
  • and refusal to sign the informed consent.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

231 participants in 2 patient groups

Experimental group
Experimental group
Description:
The experimental group was instructed to do mouthwash and nose rinse with the AgNPs solution.
Treatment:
Device: Mouthwash and nose rinse with the AgNPs solution
Control group
Active Comparator group
Description:
The "control" group was instructed to do mouthwashes and nose rinse in a conventional way.
Treatment:
Device: Mouthwashes and nose rinse in a conventional way

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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