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临床试验/NCT07200076
NCT07200076已完成不适用

Comparison of Mean Duration of Post Operative Analgesia Following QL-2 Block vs QL-3 Block Using Ropivacain 0.25% in Patients Undergoing Unilateral Inguinal Hernia Repair

Quaid-e-Azam Medical College2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
64
试验地点
2
主要终点
Change in systolic Blood pressure

研究概览

简要总结

To compare the mean dulation of post operative analgesia following QL2 block (posterior quadratus lumborum block) and the QL3 block (transmuscular quadratus lumborum block) using ropivacaine 0.25% in patients undergoing unilateral inguinai hernia repair.

Rationale of the proposed study is to find an optimal approach for quadratus lumborum block (QLB) in the context of local population as no local study has already been carried out for our population. The study seeks to determine which approach provides superior postoperative pain relief and aspires to establish a clear rationale for the application of one technique over the other in local population. By uncovering the strengths and limitations of each approach, the study intends to guide local clinicians in making informed decisions for optimizing postoperative pain management strategies. The outcomes of this study are anticipated to have a substantial impact on clinical practice, potentially leading to improved patient outcomes, reduced opioid consumption, and enhanced patient comfort following inguinal hernia repair surgeries in local settings.

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
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 50 years ASA status 1 or 2 Scheduled for unilateral inguinal hernia repair under General Anaesthesia

排除标准

  • Patient refusal Patients with pre-existing coagulation abnormalities INR more thnn 1.5 Patients with Strangulated hernia Hypersensitivity to local anaestiretics. Local infection at procedure sito.

结局指标

主要结局

Change in systolic Blood pressure

时间窗: Baseline, 30 minutes, 2 hours, 4 hours, 8 hours, 12 hours 24 hours

Mean duration of analgesia

时间窗: Baseline, 30 minutes, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours

assessed using the Visual Analog Score (VAS) ranging tiom 0-10 (0= no pain, l0= the most severe unbearable pain)

次要结局

未报告次要终点

研究者

发起方
Quaid-e-Azam Medical College
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Muhammad Ayaz

Principal investigator

Quaid-e-Azam Medical College

研究点 (2)

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