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临床试验/NCT06948383
NCT06948383进行中(未招募)不适用

Serratus Posterior Superior Intercostal Plane Block Versus Serratus Anterior Plane Block for Breast Surgery: A Randomized Controlled Trial

Zonguldak Bulent Ecevit University2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
90
试验地点
2
主要终点
postoperative opioid consumption

研究概览

简要总结

The effects of the newly defined serratus posterior superior intercostal plane block and serratus anterior plane block on postoperative analgesia and quality of recovery in women undergoing breast surgery will be investigated.

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
Double (Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients who have received informed consent form Patients who will undergo Breast Cancer Surgery aged between 18-65

排除标准

  • <18 years and >65 years
  • History of allergy to local anesthetics
  • Clinical diagnosis of coagulation disorders
  • Infection near the entry site
  • Chronic analgesic use Patients who will undergo bilateral Breast Cancer Surgery
  • Body mass index >35
  • Clinical diagnosis of Dementia or confusion
  • Lack of cooperation

结局指标

主要结局

postoperative opioid consumption

时间窗: up to 24 hour after surgery

total opioid consumption during postoperative 24 hours

次要结局

  • Postoperative pain scores(postoperative 2nd 6th, 12th 24th hour)
  • quality of recovery(postoperative 24 hour)

研究者

发起方
Zonguldak Bulent Ecevit University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Merve Sena BAYTAR

Principal Investigator

Zonguldak Bulent Ecevit University

研究点 (2)

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