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临床试验/NCT03663426
NCT03663426已完成不适用

Randomized Controlled Trial Study in Hip Arthroplasty by Direct Anterior Approach Using Opioid Free Anesthesia (OFA) Versus Standard Opioid Anesthesia.

AZ Sint-Jan AV2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2019年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
2
主要终点
QoR15

研究概览

简要总结

all patients with a first anterior arthroplasty, give their informed consent to be randomized to control or study protocol.

control means no high steroid dose, opioids for anesthesia; paracetamol, NSAIDs and opioids as analgesia.

study protocol means methylprednisolone 125 mg and opioid free anesthesia followed by paracetamol, NSAIDs and if needed opioids as escape.

详细描述

study group means for Anesthesia:

  1. High dose corticoids pre-operative: 125 mg Methylprednisolone. (Medrol) pre incision and 24h postoperative
  2. OFA using a multimodal approach including alpha2agonists, lidocaine and low dose ketamine (max 1mg/kg).
  3. Avoid opioids post-operative by using multimodal non-opioid analgesics after OFA. Avoid epidural to allow rapid mobilization.

all patients get Tranexamic acid 1 g (2 amp Exacyl 500mg) before and 1 g after surgery. It act as antifibrinolytic to reduce postoperative bleeding. (reversibly binding to lysine receptor sites on plasminogen) Try to give Continuous deep neuromuscular block (NMB) with a post titanic count (PTC) < 3 by continuous infusion and monitoring of NMB.

Intravenous Fluid restrictions to 1 ml/kg/h as long as pulse pressure (or plethysmograph) variation < 20% to reduce wound edema.

The pericapsular injections of local anesthetic, provided the patient had no contraindications such as poor renal function or allergies. 100 ml Ropivacaine 0,2% (max dose 3 mg/kg) + additives (Adrenaline 2,5 cc) (Ropivacaine: max 3 mg/kg)

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • arthroplasty by anterior approach

排除标准

  • allergy or impossible to use any of the drugs included
  • revision procedure
  • major cardiovascular, pulmonary or renal insufficiency requiring planned post operative intensive care admission

结局指标

主要结局

QoR15

时间窗: measured at 24 hours after surgery.

quality of recovery (QoR15) measured by 15 questions evaluating condition of recovery) scale 0 to 15 with 0 being very bad while 15 being maximum recovery possible or equal to pre operative state.

opioids postoperative

时间窗: measured at 24 hours after surgery.

opioid use postoperative at 24 hours

CRP

时间窗: measured at 24 hours after surgery.

Chronic reactive protein (CRP) change 24 h post-operative

次要结局

  • length of hospital stay(until hospital discharge, maximum 7 days after surgery.)
  • complications(2 weeks postoperative)
  • surgical condition(after surgery)
  • muscle damage(after surgery)

研究者

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

Jan Mulier

head of dep anesthesia & intensive care

AZ Sint-Jan AV

研究点 (2)

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