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临床试验/NCT06422585
NCT06422585招募中不适用

Comparison of Three Different Analgesic Nerve Blocks in Total Knee Replacement Surgery

Azienda Ospedaliero, Universitaria Pisana1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
180
试验地点
1
主要终点
NRS

研究概览

简要总结

The goal of this observational study is to compare the equivalent analgesic efficacy of three regional anesthesia techniques in total knee replacement surgery. The main question it aims to answer is:

• Non inferiority of each technique in relation to the others Participants will receive selective spinal anesthesia and the antalgic nerve block depending on the group they happen to be in.

Researchers will compare the Femoral Nerve Group+IPACK block, the Saphenous Nerve block+IPACK and the Subsartorial Block groups to see if there is any difference in the pain control in the 24 hours after the surgery.

详细描述

After adequate venous access is obtained, a light sedation with Midazolam 1-2 mg is administered. The patient will be monitored and a selective spinal anesthesia will be performed. After the neuraxial procedure the antalgic block of choice is performed with about 40 mL of long acting local anesthetic.

Magnesium Solfate 1g and Dexametasone 4mg are administered after the block. If the patient wishes, a propofol continuos infusion may be administered for sedation during the surgery. Before the patient leaves the OR, Ketorolac 30mg will be administered.

Pain control after surgery will be achieved with acetaminophen 1g t.i.d., Ketorolac 30mg on demand, and Morphine solfate if NRS >5 after Ketorolac.

Every 6 hours the patient will be monitored by the anesthesia team. After 24 hours the antalgic effect of the nerve block is reasonably thought to be over, so the follow up is interrupted.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

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

入选标准

  • Age > 18 y/o
  • Total knee replacement elective surgery
  • Informed consent

排除标准

  • Age < 18 y/o
  • Surgery with general anesthesia
  • Patients with coagulopaties
  • Patients in chronic opioid therapy
  • Refuse to sign informed consent form
  • Unable to sign informed consent form
  • Know allergies to medication used for analgesia

结局指标

主要结局

NRS

时间窗: Baseline, every 6 hours for the first 24 hours after surgery

To compare the analgesic effect at 24 hours, of a nerve block technique compared to others after selective spinal anesthetic is administerd to achieve surgical anesthesia.Evaluate pain for every group in the first 24 hours post surgery using the Numeric Pain Scale (NRS) assigning a numeric value between zero (no pain) and ten (the worst pain ever felt). Absence of relevant pain is considered a NRS less than three. Success of the block was defined as NRS≤3.

次要结局

  • side effect(24 hours)

研究者

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

Serena Ricalzone

principal investigator

Azienda Ospedaliero, Universitaria Pisana

研究点 (1)

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