se of saliva for screening patients with COVID-19

• Conditions: Coronavirus Infections; 37050

• Registration Number: RBR-5sw6sjz
• Lead Sponsor: Instituto Federal do Paraná

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-06-30
• Study Start: 2021-07-07
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Case group: adult adults; 20 to 45 years; the city of Londrina; without comorbidities; non-smoking; of both sexes; with symptoms for CODIV-19; assisted at the Sabará-Londrina Emergency Care Unit.
Control group: adult adults; 20 to 45 years; the city of Londrina; without comorbidities; non-smoking; of both sexes; no symptoms for CODIV-19.

Exclusion Criteria

Case group: volunteers who present comorbidities during the execution of the research; who start to use medication for continuous use that interferes with the quantity and quality of saliva; who in the course of the research are hospitalized for the treatment of the disease or give up participating in the research.
Control group: volunteers who present comorbidities during the execution of the research; who start to use medications for continuous use that interfere in the quantity and quality of saliva; and that in the course of the research they are tested positive for COVID-19 or who quit participating of the research.

Study & Design

• Study Type: Observational
• Study Design: Not specified