Trials / Unknown
UnknownNCT04887233
Efficacy and Safety of Longan Extract Spray (P80 Spray) in Volunteers With Coronavirus Disease 2019 (COVID-19)
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Chulalongkorn University · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The objectives of this study are to evaluate efficacy and safety of longan extract spray (P80 spray) in volunteers with coronavirus disease 2019 (COVID19).Patients who infected COVID 19 (positive COVID 19 RT-PCR from nasal swab) are enrolled in the study. They will be treated with standard treatment of COVID 19. In addition, the patients will received longan extract nasal spray (P80 spray) or placebo nasal spray for 3 days (6 times). After that, they will be nasal swabbed for detecting COVID 19 infection. Adverse event will also be evaluated by physician or nurse.
Detailed description
Patients who infected COVID 19 (positive COVID 19 RT-PCR from nasal swab) and pass inclusion criteria are enrolled in the study. The patients will be checked the clinical symptoms and chest x-ray by physician. They will be treated with standard treatment of COVID 19. In addition, the patients will received longan extract nasal spray (P80 spray) or placebo nasal spray for 3 days (6 times). Physician or nurse will ask for adverse events every day. After 3 days, the patients will be nasal swabbed for detecting COVID 19 infection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Longan nasal spray | The patients will be received 2 puff of Longan nasal spray 2 times/day for 3 days. |
| OTHER | Placebo | The patients will be received 2 puff of placebo nasal spray 2 times/day for 3 days. |
Timeline
- Start date
- 2021-07-01
- Primary completion
- 2022-05-31
- Completion
- 2022-06-30
- First posted
- 2021-05-14
- Last updated
- 2021-05-17
Source: ClinicalTrials.gov record NCT04887233. Inclusion in this directory is not an endorsement.