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临床试验/NCT06265441
NCT06265441已完成不适用

Comparison of IPACK Block With Adductor Canal Block vs Adductor Canal Block Alone for Post Operative Analgesia Following Arthroscopic Knee Surgeries

Ain Shams University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Assessment of pain using the visual analogue scale (VAS) at 2 hours, 4 hours, 6 hours, and 8 hours after the completion of the surgical procedure and skin closure.

研究概览

简要总结

In this study, the invistigators aim to compare postoperative analgesia effectiveness between combined interspace between the popliteal artery and posterior capsule of the knee block (IPACK) and Adductor canal block vs. Adductor canal block alone after Arthroscopic knee surgeries focusing on VAS score assessment at 8 hours postoperative.

详细描述

Patients who fulfilled the inclusion criteria and agreed to participate in the study will be randomly divided into two groups using their computer-generated random numbers such that even numbers will be enrolled in group A for Adductor canal block alone and odd numbers will be enrolled in group B for Adductor canal block and IPACK block.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Physical status: ASA 1 or 2 and candidates for spinal anesthesia undergoing Arthroscopic knee surgery.
  • Age group: 20-40 years.
  • No sex predilection.

排除标准

  • Patient refusal
  • Physical status: ASA III or above.
  • Patients with contraindications for spinal anaesthesia.
  • Patients with history of drug allergies to study drugs.
  • Evidence of local infection at site of injection.
  • Neuromuscular pathology (example: - Multiple Sclerosis)

结局指标

主要结局

Assessment of pain using the visual analogue scale (VAS) at 2 hours, 4 hours, 6 hours, and 8 hours after the completion of the surgical procedure and skin closure.

时间窗: 8 hours

Visual analogue scale (VAS) (scale 0-10, where 0 = no pain and 10 = worst imaginable pain). All the patients will have the VAS score explained and taught for self-assessment of pain at the time of enrolment for the study.

次要结局

  • The number of steps(24 hours)
  • Total pethidine consumption(24 hours)
  • The time till first analgesic requirement(as requested by patient)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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