跳至主要内容
临床试验/NCT07320781
NCT07320781已完成不适用

Role of Preoperative Tapentadol in Reduction of Perioperative Analgesic Requirement After Breast Conservative Surgery in Cancer Patients.

Shaukat Khanum Memorial Cancer Hospital & Research Centre1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年11月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
70
试验地点
1
主要终点
Intraoperative and postoperative morphine consumption

研究概览

简要总结

This study evaluated the preemptive analgesic efficacy of Tapentadol in reducing peri operative analgesic requirements among patients undergoing breast cancer surgery.

详细描述

A double blinded prospective RCT was conducted with 70 patients undergoing breast cancer surgery with 35 patients being studied with Administrated drug & other 35 as placebo. Intraoperative & postoperative morphine consumption was calculated and documented.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Care Provider)

盲法说明

The patient and doctor providing anesthesia were blinded.

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 18-60 years
  • Patients scheduled for breast conservation surgery -

排除标准

  • Patient refusal
  • CKD greater than 3
  • BMI greater than 35
  • Known drug allergy -

研究组 & 干预措施

Tapentadol

Active Comparator

Control drug (Tapentadol )

干预措施: Tapentadol (Drug)

Placebo

Placebo Comparator

Placebo sodium bicarbonate/ peppermint oil tablet

干预措施: Placebo (Other)

结局指标

主要结局

Intraoperative and postoperative morphine consumption

时间窗: During the course of surgery and up to 4 hours surgery

During the course of surgery and up to 4 hours surgery Intraoperative and postoperative morphine consumption.

次要结局

未报告次要终点

研究者

发起方
Shaukat Khanum Memorial Cancer Hospital & Research Centre
申办方类型
Other
责任方
Sponsor

研究点 (1)

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