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临床试验/NCT04908878
NCT04908878已完成不适用

Analgesic Efficacy of Combined Ultrasound-Guided PECS II and Transeversus Thoracic Plane Blocks Versus Ultrasound-Guided Serratus Anterior Plane Block in Modified Radical Mastectomy: A Prospective Randomized Study

Tanta University1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2021年6月1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
入组人数
70
试验地点
1
主要终点
The total amount rescue analgesic consumption (morphine) in the first 24 hours postoperatively.

研究概览

简要总结

The aim of this study is to evaluate the analgesic efficacy of combined ultrasound (US)-guided pectoral nerve (PECS) block II and transversus thoracic plane (TTP) block versus US-guided serratus anterior plane (SAP) block in female patients undergoing modified radical mastectomy.

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 (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •Female patients
  • •Aged 21-60 years
  • •ASA physical status I, II
  • •Scheduled for unilateral modified radical mastectomy

排除标准

  • •Patient refusal.
  • •Known hypersensitivity to local anesthetics.
  • •Body mass index > 35 kg /m
  • •Uncooperative or psychiatric patients.
  • •Infection at the injection site.
  • •Coagulation disorder.

研究组 & 干预措施

Group I (pectoral nerve (PECS) block -transversus thoracic plane (TTP) block group)

Experimental

Patients will receive unilateral US-guided PECS II block and TTP block on the side of the operation after induction of general anesthesia.

干预措施: Pectoral nerve (PECS) block -transversus thoracic plane (TTP) block (Procedure)

Group II (serratus anterior plane (SAP) block group)

Experimental

Patients will receive US-guided SAP block after induction of general anesthesia.

干预措施: Serratus anterior plane (SAP) block (Procedure)

结局指标

主要结局

The total amount rescue analgesic consumption (morphine) in the first 24 hours postoperatively.

时间窗: First 24 hours postoperatively.

Rescue analgesia in the form of morphine (3mg IV) will be given if the VAS is ≥ 40, repeated with lock out interval of 5 min guided with the occurrence of complications till the VAS is decreased to less than 40.

次要结局

  • The degree of postoperative pain(First 24 hours postoperatively.)
  • Intraoperative fentanyl consumption.(Intraoperative)
  • Time to first rescue analgesia request.(First 24 hours postoperatively.)

研究者

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

Alshaimaa Soliman Alasrag

Resident at Anesthesiology, Surgical ICU and Pain medicine

Tanta University

研究点 (1)

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