PACTR202102535686338尚未招募3 期
A Multi-Center, Open-Label, Randomized, Controlled Clinical Trial of the Efficacy of Ivermectin for the Treatment and Prophylaxis of COVID-19
agos State Ministry of Health0 个研究点目标入组 240 人开始时间: 2021年2月14日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 240
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- All
入选标准
- •In order to be eligible to participate in this study, a patient must meet all of the following criteria:
- •(1) Provide written informed consent prior to initiation of any study procedures
- •(2) Understand and agree to comply with planned study procedures
- •(3) Agree to the collection of nasopharyngeal swabs, sputum, and venous blood per protocol
- •(4) Be a male or non-pregnant female adult =18 years of age at the time of enrolment
- •(5) Have laboratory-confirmed SARS-CoV-2 infection as determined by RT-PCR in any specimen no more than 7 days prior to randomization OR be a household contact (within 7 days) of an individual with lab positive COVID-19 disease.
排除标准
- •An individual who meets any of the following criteria will be excluded from participation in this study:
- •1. Stage 4 severe chronic kidney disease or requiring dialysis (eGFR < 30)
- •2. Pregnant or breastfeeding.
- •3. Anticipated transfer to another facility that is not a study site within 72 hours.
- •4. Participants with known haematological diseases (G6PD deficiency)
- •5. Participants with chronic liver and kidney disease and reaching end-stage.
- •6. Participants with arrhythmia and chronic heart disease.
- •7. Participants known to have or hearing loss.
- •8. Participants known to have a mental disability.
- •9. Skin disorders (including rash, dermatitis, psoriasis).
- •10. Allergy to Ivermectin or its analogues.
- •11. Participants known to have filaria.
研究者
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