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临床试验/NCT05613101
NCT05613101已完成不适用

Comparison of the Effects of Ultrasound-Guided Erector Spinae Plane Block and Adductor Canal Block on Postoperative Pain, Opioid Consumption and Quadriceps Muscle Strength in Total Knee Arthroplasty Surgery

Istanbul Medeniyet University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年12月15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
40
试验地点
1
主要终点
Postoperative pain 48. hour

研究概览

简要总结

Total knee arthroplasty surgery is preferred in the treatment of osteoarthritis and causes severe postoperative pain. In this study, we aimed to investigate the effects of lumbar erector spina plan block and adductor canal block on postoperative pain and quadriceps muscle strength in patients who underwent total knee arthroplasty with spinal anesthesia.

详细描述

In a prospective, randomized study; Medeniyet University Faculty of Medicine Göztepe Prof. Dr. Forty patients who underwent total knee arthroplasty surgery at Süleyman Yalçın City Hospital were divided into two groups. After the surgery was completed, erector spina plane block was applied to Group E (n=20) patients with 20 ml of 0.25% bupivacaine from the operated side L3-L4 level, while in Group A (n=20) patients, in the area where the sartorius muscle crosses the adductor magnus muscle, it was lateral to the superficial femoral artery. Adductor canal block was applied to the adductor canal with 20 ml of 0.5% bupivacaine. All patients were administered 1 gr paracetamol and 75 mg diclofenac sodium when their pain started in the orthopedic ward. Numerical pain score and quadriceps muscle strength were evaluated during the 48-hour follow-up of the patients. When the pain score was 4 and above, 50 mg pethidine hydrochloride was administered.

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
Double (Care Provider, 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

  • patients who underwent total knee arthroplasty surgery
  • ASA I-III patients

排除标准

  • Patients with coagulopathy
  • Patients history with local anesthetic allergy or toxicity
  • Patients with long hospital stay
  • Patients with advanced organ failure
  • Mental retarded patients
  • Presence of infection at the injection site

结局指标

主要结局

Postoperative pain 48. hour

时间窗: 48. hour

Visual anolog score (1-10)

Postoperative pain 1. hour

时间窗: 1. hour

Visual anolog score (1-10)

Postoperative pain 30 minute

时间窗: 30. min.

Visual anolog score (1-10)

Postoperative pain 2. hour

时间窗: 2. hour

Visual anolog score (1-10)

Postoperative pain 6. hour

时间窗: 6. hour

Visual anolog score (1-10)

Postoperative pain 12. hour

时间窗: 12. hour

Visual anolog score (1-10)

Postoperative pain 24. hour

时间窗: 24. hour

Visual anolog score (1-10)

Postoperative pain 36. hour

时间窗: 36. hour

Visual anolog score (1-10)

次要结局

  • Opioid consuption 30. min.(30. min.)
  • Opioid consuption 6. hour(6. hour)
  • Opioid consuption 12. hour(12. hour)
  • Opioid consuption 36. hour(36. hour)
  • Opioid consuption 1. hour(1. hour)
  • Opioid consuption 2. hour(2. hour)
  • Opioid consuption 24. hour(24. hour)
  • Opioid consuption 48. hour(48. hour)

研究者

发起方
Istanbul Medeniyet University
申办方类型
Other
责任方
Principal Investigator
主要研究者

İnal Bensu Arıoglu

Medical Doctor

Istanbul Medeniyet University

研究点 (1)

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