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临床试验/NCT06188806
NCT06188806招募中不适用

Investigation of the Effect of Proximal and Distal Adductor Canal Block on Pain Control and Functional Mobility in Total Knee Prosthesis Surgery Performed Under Spinal Anesthesia

Umraniye Education and Research Hospital2 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2023年11月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
78
试验地点
2
主要终点
VISUAL ANALOGUE SCALE(VAS)

研究概览

简要总结

to investigate the effect of adductor canal block applied with two different approaches in the treatment of pain after TKA surgery on pain control and functional mobility.

详细描述

This prospective randomized trial is randomly divided into 3 groups using the method. Total knee arthroplasty is performed by the same surgical team.

is applied. The patients were divided into proximal ACB applied, distal ACB applied and control groups.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Medications for unilateral TKA surgery
  • Patients aged 18-85

排除标准

  • Patients under 18 years of age and over 85 years of age
  • Patients with ASA 4 and above
  • Patients with cognitive impairment
  • Patients with application site infection
  • Patients allergic to local anesthesia
  • Patients receiving anticoagulant therapy
  • Patients with bleeding diathesis
  • Patients with chronic opioid or substance use
  • Patients with insulin-dependent diabetes mellitus
  • patients with neuropathy
  • patients with hepatic or renal failure
  • Patients who do not accept the procedure to be applied

结局指标

主要结局

VISUAL ANALOGUE SCALE(VAS)

时间窗: POSTOPERATIVE 6, 12 AND 24 HOURS

VAS pain score was evaluated as "no pain" (score=0) and "worst pain" (score=10) and was divided into 3 groups according to the World Health Organization's pain intensity scale: score \<3 mild pain, 3-6 mild-moderate. degree pain and \>6 moderate-severe pain.

次要结局

  • first mobilization time(within postoperative 24 hours)
  • length of hospital stay(ONE WEEK)
  • opioid use(within postoperative 24 hours)

研究者

发起方
Umraniye Education and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Zeliha Alicikus

head of Anesthesia and reanimation

Umraniye Education and Research Hospital

研究点 (2)

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