Official Title
Efficacy of a Nasal Spray Containing Iota-Carrageenan in the Prophylaxis of COVID-19 Disease in Health Personnel Dedicated to Patients Care With COVID-19. Multicenter, Randomized, Double-blind, Placebo-controlled Trial (CARR-COV-02)
Brief Summary

Coronaviruses are enveloped viruses with an RNA genome. Carrageenans are sulfate polysaccharides synthesized by red algae. Studies conducted in adults and children with the common cold showed the effectiveness of the use of Carrageenan in nasal spray. For decades, the antiviral action of Carrageenans has been described in numerous studies with different viruses that infect humans: herpes viruses types 1 and 2, human immunodeficiency virus, human papillomavirus, H1N1 influenza virus, dengue virus, rhinovirus, hepatitis A virus, and enteroviruses. Studies on the dynamics of COVID-19 disease show an intense and rapid pharyngeal multiplication in the first 3-5 days of the onset of symptoms, prior to the onset of pulmonary disease. Finally, this molecule has shown a viricidal effect against SARS-Cov2 in vitro. All this underscores the potential value of a therapy that inhibits the virus in the rhinopharynx.

Detailed Description

This is a multicenter, randomized, double-blind, placebo-controlled trial assessing the use a
nasal spray containing Iota-Carrageenan in the prophylaxis of COVID-19 disease in
health-workers.

Unknown status
COVID19

Drug: Iota-Carrageenan

Participants will received a nasal spray with Iota-Carrageenan or placebo 4 times a day during 21 days
Other Name: Placebo

Eligibility Criteria

Inclusion Criteria:

- physician, nurses, and physical therapist who usually attend hospitalized COVID19
patients.

- No more than 48 hours since he/she assisted a COVID-19 patient

- Able to understand and give written informed consent

Exclusion Criteria:

- Participation in any other clinical trial of an experimental treatment for COVID-19

- Not having a cell phone with WhatsApp for remote monitoring

- Hypersensitivity or known allergy to any component of the product

- Pregnancy or lactation

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
Argentina
Locations

centro de educación médica e investigaciones clinicas (CEMIC)
Buenos Aires, Capital Federal, Argentina

Investigator: Mónica Lombardo, MD
Contact: 541152990600
mlombardo@nobeltri.com

Contacts

Mónica Lombardo, MD
005491141763599
mlombardo@nobeltri.com

Ricardo Valentini, MD
005491162036790
deptomedicina2@gmail.com

Juan Figueroa, MD, Study Director
Instituto Milstein-CONICET

Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
NCT Number
MeSH Terms
COVID-19