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临床试验/NCT07705516
NCT07705516已完成不适用

Combined Rectus Sheath and Quadratus Lumborum Blocks Versus Quadratus Lumborum Block Alone for Movement-evoked Pain After Laparoscopic Gynecologic Surgery: a Prospective Randomized Open-label Trial

Medical and Diagnostic Center "MEDION" LLC1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年1月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Postoperative pain intensity

研究概览

简要总结

The purpose of this study is to evaluate the clinical efficacy of combining ultrasound-guided bilateral rectus sheath blocks (RSB) and quadratus lumborum blocks (QLB) compared to using a quadratus lumborum block alone for postoperative analgesia in patients undergoing laparoscopic gynecological surgeries.

The primary objective is to assess movement-evoked pain scores in the early postoperative period. Secondary objectives include the evaluation of postoperative opioid consumption, intraoperative hemodynamic stability, and the overall incidence of side effects. Investigators hypothesize that the combined interfacial abdominal wall block technique will provide superior pain relief and reduce opioid requirements during recovery.

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
None

入排标准

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

入选标准

  • Scheduled for elective gynecological video-laparoscopic surgery.
  • ASA physical status І-ІІ.
  • Age between 18 and 65 years.
  • Patient's informed consent to participate in the study

排除标准

  • Known allergy or contraindications to local anesthetics.
  • Infection at the potential needle insertion sites.
  • Coagulopathy or ongoing anticoagulant therapy.
  • Conversion to open laparotomy during surgery.
  • Severe cognitive impairment or psychiatric disorders.

结局指标

主要结局

Postoperative pain intensity

时间窗: At 2, 4, 6, 12, and 24 hours postoperative assessment

Visual Analog Scale (VAS) score. Scale from 0 to 10. 0 means no pain. 10 means worst pain. Lower scores sindicate less pain.

次要结局

  • Total opioid consumption. Postoperative period. Measured in milligrams.(Within 24 hours after surgery.)

研究者

发起方
Medical and Diagnostic Center "MEDION" LLC
申办方类型
Other
责任方
Principal Investigator
主要研究者

Slipukha Denys

Staff Anesthesiologist

Medical and Diagnostic Center "MEDION" LLC

研究点 (1)

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