Coronavirus Disease 2019 Clinical Trial
Official title:
Evaluation of KGR Prescriptions in Suppressing COVID-19 Infection.
Verified date | March 2024 |
Source | China Medical University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
These studies offer valuable insights into the potential development of KGR as a novel herbal-based preventive and therapeutic strategy against COVID-19.
Status | Completed |
Enrollment | 26 |
Est. completion date | February 8, 2024 |
Est. primary completion date | April 18, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility | Inclusion Criteria: - Healthy participants aged 20-60 with a body weight of over 50 kilograms. - Individuals who have never been diagnosed with COVID-19 or have recovered from COVID-19 for more than three months. - No consumption of any traditional Chinese medicine or food containing Chinese medicine within the preceding 36 hours before the experiment. - Vaccinated individuals who received their vaccine more than three months ago. - Willingness to undergo venous blood tests (approximately 10 cc of blood to be drawn three times). Exclusion Criteria: - History of major internal medical conditions, including diabetes, hypertension, chronic obstructive pulmonary disease (COPD), asthma, abnormal liver function (AST levels exceeding 5 times the normal value), renal dysfunction (eGFR <60), cancer, etc. - Brain disorders such as trauma, stroke, tumors, epilepsy, or dementia. - Mental health disorders such as depression, anorexia nervosa, or schizophrenia. - Pregnant or lactating women. If there is suspicion of pregnancy, a commercial urine pregnancy test will be conducted. - Smokers, alcoholics, or betel nut addicts. - Inability to comply with the trial procedures. - Inability to sign the informed consent form. - Within three months of a confirmed COVID-19 diagnosis. - Within three months of receiving a vaccine shot. |
Country | Name | City | State |
---|---|---|---|
Taiwan | China Medical University Hospital | Taichung | North District |
Lead Sponsor | Collaborator |
---|---|
Sheng-Teng Huang |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Serum Infection rate of pseudocells | Collected Blood, centrifuge to obtain serum samples. Each serum sample were diluted and premixed with wild-type or different variants of SARS-CoV-2 spike Vpps for one hours before incubation with 293T-ACE2 cells. After 24 hours of infection, the infection efficiency rate was measured according to luciferase activities. | Before taking, 2 hours after taking, and 2 hours after taking 24 hours later. |
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