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临床试验/NCT01891435
NCT01891435已完成不适用

A Randomized Controlled Clinical Trial on the Antipyretic Efficacy of Oral Paracetamol, Intravenous Paracetamol and Intramuscular Diclofenac in Patients Presenting With Fever to Emergency Department

Hamad Medical Corporation1 个研究点 分布在 1 个国家目标入组 434 人开始时间: 2010年1月最近更新:
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
434
试验地点
1
主要终点
Reduction in temperature in every thirty minutes till 120 minutes after receiving antipyretics

研究概览

简要总结

A randomized clinical trial to check the antipyretic efficacy of oral and intravenous paracetamol and intramuscular diclofenac sodium in patients presenting with fever to emergency department.

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
14 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults between the age of 14-75 years with an oral temperature of more than 38.5 C

排除标准

  • History of allergy to any of the drugs in the study
  • Had taken antipyretics within 8 hours
  • Renal, hepatic or haematological disorders
  • bronchial asthma, peptic ulcer disease, vomiting
  • Pregnant or lactating women

研究组 & 干预措施

oral paracetamol

Active Comparator

patients in this arm will receive 1000mg of oral paracetamol

干预措施: Oral paracetamol (Drug)

Intravenous paracetamol

Active Comparator

patients in this arm will receive 1000 mg of intravenous paracetamol

干预措施: Intravenous paracetamol (Drug)

Intramuscular Diclofenac

Active Comparator

patients in this arm will receive 75 mg of intramuscular diclofenac sodium

干预措施: Intramuscular diclofenac (Drug)

结局指标

主要结局

Reduction in temperature in every thirty minutes till 120 minutes after receiving antipyretics

时间窗: Reduction in temperature is checked every 30 minutes for a maximum of 120 minutes

Once the patients fulfill the inclusion criteria, they are randomly assigned to receive one of the three medications in the study ( oral paracetamol, intravenous paracetamol or intramuscular diclofenac). Baseline temperature is recorded using a standard thermometer. Then reduction in temperature is recorded every 30 minutes for 2 hours.

次要结局

未报告次要终点

研究者

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

Firjeeth C Paramba

Specialist, Emergency Department

Hamad Medical Corporation

研究点 (1)

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