IRCT20200509047364N3尚未招募3 期
Evaluation of the efficacy of N-Acetylcysteine in severe COVID-19 patients: a randomized controlled phase III clinical trial
Bandare-abbas University of Medical Sciences0 个研究点目标入组 40 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
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
- no limit 至 no limit（—）
- 性别
- All
入选标准
- •All COVID-19 patients whose disease has been confirmed by the PCR test for SARS-Cov-2.
- •Having one of the criteria for severe COVID-19 disease includes tachypnea (respiration rate> 30 per minute), hypoxemia (O2 = saturation, arterial oxygen partial pressure ratio <300), pulmonary infiltration (> 50% of lung area during 24 48 h), LDH> 245 U / l, Progressive lymphopenia.
- •Hospitalized in the intensive care unit.
- •Signing the written consent of the study participant.
排除标准
- •Known allergy or hypersensitivity to N-Acetylcysteine.
- •The participant refused to participate in the continuation of the study.
研究者
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