Evaluation of mouthwash, mouth spray, and nasal spray as treatment of COVID-19 patients and prevention of individuals at risk of exposure to COVID-19 infectio

Phase 3

• Conditions: COVID-19; mouthwash, mouth spray, nasal spray, COVID-19 infection

• Registration Number: TCTR20240803002
• Lead Sponsor: Silpakorn University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2022-08-04
• Study Start: 2024-08-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1. Be 18 years of age or older on the date of submitting the consent form.
2. Women must not be pregnant or breastfeeding.
3. If you are a married woman of reproductive age, you must use birth control for at least 1 month before entering the trial. Acceptable birth control methods include taking birth control pills, injections, birth control rings, birth control implants, or using condoms. This must continue until the experiment is completed.
4. Do not drink alcohol or smoke.
5. You must not be in the process of losing weight and must have no history of allergies to drugs, cosmetics, chemicals, or natural extracts.
6. Volunteers will receive training on product use and detailed information about the consent documentation.

Exclusion Criteria

1. Project participants have a serious illness (acute illnesses) or require hospitalization within 3 days of joining the project.
2. Participants have used other nasal sprays, especially steroids, in the past 7 days.
3. Project participants have previously undergone a tracheotomy (tracheostomy).
4. Project participants are receiving oxygen therapy.
5. Females who are breastfeeding, pregnant, or intending to become pregnant.
7. People with mental or nervous system disabilities that prevent independent use of the product.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
cough 7 days 5-point Likert scale,sore throat 7 days 5-point Likert scale,runny nose 7 days 5-point Likert scale

Secondary Outcome Measures

Name	Time	Method
Satisfaction 7 days 5-point Likert scale