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临床试验/NCT05509244
NCT05509244招募中不适用

Efficacy of Acetaminophen-ibuprofen Combination on the Postoperative Pain After Laparoscopic Gynecology Surgery

The Catholic University of Korea1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2022年9月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
64
试验地点
1
主要终点
postoperative pain

研究概览

简要总结

Acetaminophen and ibuprofen has been safely used for a long time and reduces postoperative pain and opioid dosages. Investigators are planning to compare the efficacy of 1) acetaminophen only and 2) acetaminophen and ibuprofen combination at postoperative pain after laparoscopic gynecologic surgery.

详细描述

Acetaminophen and ibuprofen has been safely used for a long time and reduces postoperative pain and opioid dosages. Investigators are planning to compare the efficacy of 1) acetaminophen 1g only and 2) the combination of acetaminophen 1g and ibuprofen 300mg at postoperative pain after laparoscopic gynecologic surgery. Some recovery valuables such as the postoperative pain and opioid requirements will be assessed.

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients scheduled gynecologic laparoscopic surgery

排除标准

  • Refusal to be enrolled in the study
  • Emergency surgery
  • On chronic pain medications
  • Psychiatric disorders
  • Pregnant, lactating women
  • Allergy or contraindication to the medication drugs

研究组 & 干预措施

control group

Active Comparator

acetaminophen 1g iv dripping

干预措施: Acetaminophen (Drug)

experimental group

Experimental

the combination of acetaminophen 1g and ibuprofen 300mg iv dripping

干预措施: Acetaminophen (Drug)

experimental group

Experimental

the combination of acetaminophen 1g and ibuprofen 300mg iv dripping

干预措施: Ibuprofen (Drug)

结局指标

主要结局

postoperative pain

时间窗: during 30 minutes after surgery

the maximal postoperative pain severity using pain scale (0=no pain; 10=the worst pain)

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

Young Eun Moon

professor

The Catholic University of Korea

研究点 (1)

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