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临床试验/NCT07246720
NCT07246720尚未招募不适用

Interpectoral-pectoserratus Plane Block vs. Serratus Posterior Superior Intercostal Plane Block for Postoperative Analgesia in Patients Undergoing Breast Cancer Surgery

Zonguldak Bulent Ecevit University1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025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
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Cumulative opioid consumption

研究概览

简要总结

This prospective, randomized clinical study aims to compare the analgesic efficacy of the interpectoral-pectoserratus plane block and the serratus posterior superior intercostal plane block for postoperative pain management in patients undergoing breast cancer surgery. Both techniques are ultrasound-guided regional anesthesia methods targeting different interfascial planes of the thoracic wall. The study will evaluate postoperative pain scores, opioid consumption, Quality of recovery and potential complications. The findings are expected to contribute to optimizing regional anesthesia strategies for enhanced recovery and improved analgesia following breast cancer surgery.

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
否

入选标准

  • •18-65 years of age
  • •ASA I-II-III risk groups
  • •Patients with informed consent
  • •Patients undergoing breast cancer surgery

排除标准

  • •Ages <18 and >65
  • •History of allergy to local anesthetics
  • •Known coagulation disorders
  • •Infection near the insertion site
  • •Chronic analgesic use
  • •Patients with diabetes mellitus and those receiving neoadjuvant chemotherapy (due to potential impairment of pain sensation)
  • •Body mass index >30
  • •Dementia or confusion
  • •Lack of cooperation

研究组 & 干预措施

Group IPP-PSP

Active Comparator

Interpectoral-Pectoserratus Plane Block

干预措施: Interpectoral-Pectoserratus Plane Block (Procedure)

Group SPSIPB

Active Comparator

Serratus Posterior Superior Intercostal Plane Block

干预措施: Serratus Posterior Superior Intercostal Plane Block (Procedure)

结局指标

主要结局

Cumulative opioid consumption

时间窗: in the first 24 hours after completion of the surgical procedure

Cumulative opioid consumption in the first 24 postoperative hours after the completion of the surgical procedure

次要结局

  • Postsurgical Quality of Recovery measured by the Quality of Recovery questionnaire(first day after surgery)
  • Number of episodes of postoperative pain(In the first 24 hours after completion of the surgical procedure)

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

Çağdaş Baytar

medical doctor

Zonguldak Bulent Ecevit University

研究点 (1)

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