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临床试验/NCT07046390
NCT07046390尚未招募不适用

Comparative Study Between Triple Injection Peri-Sartorius (TIPS) Block Versus Intravenous Analgesia for Postoperative Analgesia After Knee Arthroscopy

Ain Shams University1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2025年7月20日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
52
试验地点
1
主要终点
postoperative analgesics

研究概览

简要总结

In this study participants are aiming to compare triple injection peri-sartorius (TIPS) block versus intravenous analgesia for postoperative analgesia after knee arthroscopy regarding efficacy of pain relief and early ambulation

详细描述

Arthroscopic knee surgery is a commonly performed orthopedic procedure due to being minimally invasive and providing early recovery. A significant number of patients have severe postoperative pain despite using small incisions leading to poor quality of postoperative recovery. Currently, multimodal analgesia is a widely used method of pain relief and also to improve patient functionality and satisfaction scores. Systemic opioids and non-steroidal anti-inflammatory drugs (NSAIDs) have been the mainstay for treating postoperative pain after knee surgery. The traditional high-dose opioid approach is associated with increased opioid-related side effects eg: (Nausea ,vomiting and delayed recovery ).NSAIDs are effective as part of a multimodal analgesic approach, but their use can be limited due to concerns regarding coagulopathy or impairment of renal function and GIT side effects.Ultrasound guidance in regional anaesthesia is increasingly being used leading to approaches to the sciatic nerve block, femoral nerve block (FNB), adductor canal block (ACB) and obturator nerve block increasingly motivated as an element of multimodal analgesia regimen in many operations, including knee arthroscopy.Sub sartorial block has been studied for its efficacy in providing analgesia following knee surgeries while preserving quadriceps muscle power. However, misnomers have been prescribed at different locations for different block approaches. TIPS block targets motor-sparing analgesia through injection at three planes ultrsound guided.Study Procedures: Patients will be enrolled in this randomly allocated using computer-based randomization into two groups with (26) patients in each group

  • Group 1 (study group number 1) will receive triple injection peri-sartorius (TIPS) block. The block will be done after induction of general anesthesia before skin incision
  • Group 2 (study group number 2) (control group )will receive conventional analgesic regimen without having a regional 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
Single (Participant)

入排标准

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

入选标准

  • .Age 18-40 years undergoing knee arthroscopy. .Sex: Both sexes.
  • .American Society of Anaesthesiologists (ASA) Physical Status Class I and II

排除标准

  • .Declining to give written informed consent. .History of allergy to the medications used in the study. .Contraindications to regional anesthesia (including patient refusal, coagulopathy and local infection).
  • Psychiatric disorder. .American Society of Anesthesiologists (ASA) Physical Status Class III and IV.
  • Patients with body mass index (BMI) >35 kg/m2 .Neurological deficits or mobility-related disorders of the non-operated limb .
  • Moderate to severe hepatic , renal diseases and cardiac disease.

研究组 & 干预措施

tips block group

Active Comparator

this group will receive triple injection peri-sartorius (TIPS) block. The block will be done after induction of general anesthesia before skin incision

干预措施: nerve block with bupivacaine 0.25% (Drug)

tips block group

Active Comparator

this group will receive triple injection peri-sartorius (TIPS) block. The block will be done after induction of general anesthesia before skin incision

干预措施: No intervention (Drug)

结局指标

主要结局

postoperative analgesics

时间窗: 24 hours postoperative

次要结局

  • The secondary outcomes will be the total morphine consumption in mg , ambulation distances during the first 24 hours postoperative in meters(24 hours postoperative)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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