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临床试验/NCT05487001
NCT05487001已完成不适用

Analgesic Effect of Dexamethasone as a Perineural Adjuvant for Continuous Femoral Nerve Block After Total Knee Arthroplasty: a Prospective Randomized Placebo-controlled Trial

Gangnam Severance Hospital2 个研究点 分布在 2 个国家目标入组 18 人开始时间: 2022年8月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
2
主要终点
Maximum Numeric rating scale pain score at movement

研究概览

简要总结

An alternative to improve the quality of postoperative analgesia is to use various perineural adjuvants applicable to peripheral nerve block along with local anesthetics to increase the analgesic effect. Dexamethasone is a strong and long-acting corticosteroid, which reduces postoperative nausea and vomiting and increases the duration of nerve blockade. Most of the existing clinical studies compared the analgesic effect with the placebo group after adding an adjuvant in a single shot nerve block, and there were very few cases of comparing the analgesic effect with the placebo group after adding the adjuvant in peripheral nerve block through continuous catheter infusion. Therefore, we designed this study to investigate whether the use of dexamethasone as a peripheral adjuvant for continuous femoral nerve block has a better pain and recovery profile.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients 19 years of age or older who are expected to undergo unilateral hip arthroplasty

排除标准

  • Revision total hip arthroplasty
  • Allergy to drugs used in the study
  • Patients with moderate or more hepatic impairment (AST/ALT is more than 2.5 times the upper limit of normal)
  • Estimated glomerular filtration rate < 30 mL/min/1.73m2
  • Opioid dependence
  • Prolongation of PT and aPTT more than twice the upper limit of normal
  • Pre-existing neurological or anatomical disorders of the lower extremities
  • Serious psychiatric disorders

研究组 & 干预措施

sham group

Sham Comparator

sham block before surgery

干预措施: sham group (Procedure)

结局指标

主要结局

Maximum Numeric rating scale pain score at movement

时间窗: within postoperative day 2

Pain intensity at movement will be evaluated by an 11-point numeric rating scale (NRS: 0 = no pain, 10 = worst imaginable pain) postoperative 1 hour, postoperative 6 hours, postoperative day 1, postoperative day 2. Maximum Numeric rating scale pain score was determined based on highest score among repeated assessment of surgical site pain severity postoperatively.

次要结局

  • Numeric rating scale pain score at rest(up to postoperative day 2)
  • Postoperative opioid consumption(up to postoperative day 2)
  • Numeric rating scale pain score at movement(up to postoperative day 2)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Myoung Hwa Kim

Associate professor

Gangnam Severance Hospital

研究点 (2)

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