Efficacy, Safety, and Tolerability Topical Nasal Spray in the Prevention of SARS-CoV-2 Infection in Healthcare Personnel

Efficacy, Safety, and Tolerability Topical Nasal Spray in the Prevention of SARS-CoV-2 Infection in Healthcare Personnel

Efficacy, Safety, and Tolerability Topical Nasal Spray in the Prevention of SARS-CoV-2 Infection in Healthcare Personnel

Recruiting
18-90 years
All
Phase 2
  • Simplified description (AI rewritten)
  • Technical description (Original)
Treatment: Participants will be randomized to either quinine or placebo group (saline or salt water) at a 2:1 ratio. 
 Duration of the Study: Participants will self-administer study drug three times daily (TID) for 4 weeks. A follow-up visit will be made at 6 weeks to assess participant health since some cases of SARS-CoV-2 infection may not be apparent until after the treatment period has ended.

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Study details
    covid-19
    healthcare workers

NCT04408183

19 February 2024

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