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临床试验/NCT07343570
NCT07343570尚未招募3 期

Comparing Ultrasound-guided Lateral Quadratus Lumborum Block Versus Combined Ilio-inguinal/Ilio-hypogastric /Genitofemoral Block for Postoperative Analgesia After Open Inguinal Hernia Repair: A Double-blind Randomized Controlled Trial

Al-Azhar University1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2026年1月28日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
66
试验地点
1
主要终点
Cumulative opioid consumption in the first 24 hours postoperatively

研究概览

简要总结

This double-blind randomized controlled trial aimes to compares two ultrasound-guided regional techniques-lateral quadratus lumborum block versus combined ilio-inguinal/ilio-hypogastric/genitofemoral (II-IH-GFN) block-for postoperative analgesia after elective unilateral open inguinal hernia repair under spinal anesthesia in adults.

研究设计

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

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged 18-75 years.
  • ASA physical status I-III.
  • Scheduled for elective unilateral open inguinal hernia repair under standardized spinal anesthesia.
  • Able to understand and use the Visual Analogue Scale (VAS).
  • Provided written informed consent.

排除标准

  • Allergy to local anesthetics.
  • Coagulopathy or current use of anticoagulants contraindicating peripheral nerve blocks.
  • Infection at the injection site.
  • Chronic opioid use (daily opioids >2 weeks) or chronic pain syndromes.
  • Body mass index (BMI) >40 kg/m².
  • Conversion to other surgery or bilateral repair.
  • Pregnant patients.
  • Refusal to sign informed consent.

结局指标

主要结局

Cumulative opioid consumption in the first 24 hours postoperatively

时间窗: 24 hours after surgery.

Measures the total amount of opioid analgesics (expressed as morphine milligram equivalents, MME) consumed during the first postoperative 24 hours. It reflects overall analgesic efficacy of the two block techniques.

次要结局

  • Pain intensity (VAS pain scores at rest )(24 hours postoperatively.)
  • Pain intensity (VAS pain scores at movement)(24 hours postoperatively.)
  • Time to first analgesic request(24 hours.)
  • Proportion of patients requiring rescue opioid analgesia(24 hours.)
  • Incidence of postoperative block-related complications(24 hours.)
  • Patient satisfaction score(Assessed at 24 hours postoperatively.)
  • Post-anesthesia care unit (PACU) stay duration(24 hours)
  • Total hospital stay duration(24 hours)

研究者

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

Neveen Abd El Maksoad Kohaf

Lecturer of Clinical Pharmacy

Al-Azhar University

研究点 (1)

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