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临床试验/NCT07280182
NCT07280182已完成不适用

Comparing the Early Postoperative Analgesic Effect of the Transmuscular Quadratus Lumborum Block Versus the Lumbar Plexus Block for Patients Undergoing Spiral Thighplasty Surgery

Menoufia University1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2025年12月13日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
1
主要终点
Visual analogue scale score

研究概览

简要总结

Whether trans muscular QLB provides postoperative analgesia compared with LPB after thigh lift surgery

详细描述

Adequate analgesia after spiral thigh reduction (thigh lift) is essential for early mobilization and patient satisfaction. Quadratus lumborum block (QLB) has shown analgesic efficacy comparable to lumbar plexus block (LPB) for hip area surgery with potential advantages in motor-sparing and safety

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

Computer-generated randomization in variable blocks; allocation sealed in opaque envelopes. Blocks performed by an anesthesiologist not involved in postoperative assessment. Patients and outcome assessors are blinded. Drape and opaque dressings conceal injection sites for both groups to preserve blinding

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ASA ( American Society of Anaesthesia) I-II
  • elective bilateral spiral thigh lift under general anesthesia
  • consent to regional block and trial participation

排除标准

  • Coagulopathy or therapeutic anticoagulation not meeting ASRA safety windows
  • infection at injection sites
  • allergy to local anesthetics
  • preexisting significant neuropathy
  • BMI > 35 kg/m² if impeding ultrasound visualization; renal/hepatic failure; pregnancy; inability to use NRS; chronic opioid use >60 mg oral morphine equivalents/day; contraindication to study analgesics.

研究组 & 干预措施

Group QLB

Other

Ultrasound-Guided Trans-muscular QLB

干预措施: Ultrasound-Guided Trans-muscular QLB (Other)

Group LPB

Other

Ultrasound-Guided Posterior Lumbar Plexus (Psoas Compartment) Block

干预措施: Ultrasound-Guided Posterior Lumbar Plexus (Psoas Compartment) Block (Other)

结局指标

主要结局

Visual analogue scale score

时间窗: 24 hours

Visual analogue scale score at 1st,6th,12th and 24 h (where 0 is interpreted as no pain, 1-4 mild pain, 5-6 moderate pain, 7-10 severe pain)

次要结局

  • Time for first analgesic request(24 hours)
  • Opioid consumption(24 hours)
  • Time to walk >30 (meter)(24 hours)
  • Performance Time(minutes)
  • The number of patients who develop block-related complications(24 hours)
  • the patients Satisfaction questionnaire(24 hours)

研究者

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

Amal Gouda Elsayed Safan

lecturer

Menoufia University

研究点 (1)

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