TCTR20230131004已完成2 期
A randomized controlled trial to evaluate the efficacy and safety of Clears-belong Plus in participants with long COVID (COVID-19)
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 66
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
- 20 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •1. Thai males and females aged 20 years old or above.
- •2. Previously had COVID-19 infection as confirmed by ATK or RT-PCR at least 4 weeks before screening.
- •3. Long COVID diagnosis as confirmed by a physician.
- •4. Willing to attend all the study procedures.
排除标准
- •1. Have or suspected to have penumonitis
- •2. Have at least one of the following conditions: chronic obstructive pulmonary disease, chronic lung diseases, chronic renal disease, cardiovascular diseases, cerebrovascular diseases, congenital heart diseases, psychotic disorders, hepatitis, cirrhosis, and immunodeficiency disorders
- •3. Current use of warfarin or benzodiazepines
- •4. Positive result from tetrahydrocannabinol (THC) urine test at screening
- •5. Positive result from urine pregnancy test at screening
- •6. Plan to become pregnant or breastfeeding
- •7. History of hypersensitivity to any active ingredients of Clears-belong Plus
- •8. Participating in other studies
- •9. Any other health conditions that could interfere with participation in this study based on investigator's judgement
研究者
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