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临床试验/NCT06472258
NCT06472258已完成不适用

Efficacy of Only IV Artesunate Versus IV Artesunate Plus IV Quinine in the Treatment of Severe Malaria in Children: A Comparative Study

RESnTEC, Institute of Research1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2023年3月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
104
试验地点
1
主要终点
Efficacy measurement between IV Artesunate and IV Artesunate plus IV Quinine Hydrochloride

研究概览

简要总结

The WHO recommends artesunate as the drug of choice for the treatment of severe malaria. However, the efficacy of this single drug as compared to the combined drug regimen remained questionable, and the clinical response was considered delayed or inappropriate. Therefore, this research intended to evaluate the efficacy of only IV artesunate versus IV artesunate plus IV quinine in the treatment of severe malaria in children. The findings of the study would be helpful knowing whether the two drugs, when given together, have considerable benefit over single-drug therapy when given for the same.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children admitted to the emergency department with the diagnosis of severe malaria.

排除标准

  • Children with chronic kidney disease, chronic liver disease, immunosuppressive disorders, hematological disorders, malignancies, and congenital heart disease.

研究组 & 干预措施

IV Artesunate Group

Experimental

IV Artesunate with weight appropriate dosage on 0, 12, 24 and 48 hours, and continued 12 hourly for a maximum duration of seven days. Each dose diluted in normal saline given as infusion.

干预措施: IV Artesunate (Drug)

Combination Group

Experimental

IV Artesunate with weight appropriate dose on 0, 12, 24 and 48 hours, plus IV Quinine hydrochloride in accordance to weight with loading dose 20mg salt/kg in 10% dextrose infusion followed by 10mg salt/kg infusion 8 hourly for 2 days and for 12 hourly onwards for a maximum of 7 days.

干预措施: IV Artesunate (Drug)

Combination Group

Experimental

IV Artesunate with weight appropriate dose on 0, 12, 24 and 48 hours, plus IV Quinine hydrochloride in accordance to weight with loading dose 20mg salt/kg in 10% dextrose infusion followed by 10mg salt/kg infusion 8 hourly for 2 days and for 12 hourly onwards for a maximum of 7 days.

干预措施: IV Quinine Hydrochloride (Drug)

结局指标

主要结局

Efficacy measurement between IV Artesunate and IV Artesunate plus IV Quinine Hydrochloride

时间窗: Seven days

The outcome was measured in the number of hours elapsed for an individual to become fever-free.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Muhammad Aamir Latif

Investigator

RESnTEC, Institute of Research

研究点 (1)

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