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临床试验/TCTR20240803002
TCTR20240803002Enrolling By Invitation3 期

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 infection

Silpakorn University0 个研究点目标入组 100 人开始时间: 2024年8月3日最近更新:
适应症

试验速览

阶段
3 期
状态
Enrolling By Invitation
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 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.

排除标准

  • 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.

研究者

发起方
Silpakorn University

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