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临床试验/NCT06225323
NCT06225323已完成不适用

Effect of Lidocaine Infusion on Neuraxial Opioid-induced Pruritus After Cesarean Section Double-blinded, Randomized Control Clinical Trial

Aswan University1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2024年1月29日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
136
试验地点
1
主要终点
The incidence of pruritis

研究概览

简要总结

The aim of this study is to assess the efficacy and potency of lidocaine infusion as a preventive measure on pruritus response after injection of 200 micro gram morphine with bupivacaine subarachnoid block, spinal anesthesia, in cesarean section.

详细描述

Neuraxial opioids (NO) are one of the most widely used methods for postpartum analgesia, for cesarean section analgesia, and many other surgical procedures.

The pruritus induced by NO is an unpleasant, subjective, and irritating sensation that causes scratching response.

Pruritus begins shortly after anesthesia, with the onset depending on the type, route and dosage of opioid used. Pruritus invoked by lipid-soluble opioids such as fentanyl and sufentanil is of shorter duration, and the use of the minimum or small dose from opioids in addition of local anesthetics seems to decrease the prevalence and the severity of itching. Pruritus invoked by intrathecal morphine is of longer duration and is difficult to treat. Intrathecal administration, of opioids reach peak concentrations in the cerebrospinal fluid almost immediately. ]. But, after epidural administration, there is a delay in the rise to peak concentration (10-20 min with fentanyl and 1-4 h with morphine).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Age from 20 to 40 years.
  • Weight from 50 to 90 kg.
  • Women undergoing Cesarean section.

排除标准

  • Patient with known allergies to lidocaine.
  • Preexisting pruritus.
  • Coexisting skin disorders.
  • Contraindications to spinal anesthesia.
  • Preeclampsia.
  • Eclampsia.
  • Major systemic diseases.
  • Refusal to participate.
  • Uses of any current drugs have potential effects on post-operative itching as steroidal ,nonsteroidal ,ondanstern, propofol, midazolam during study period.

研究组 & 干预措施

Lidocaine group

Experimental

Patients will receive Lidocaine infusion for 6 hours

干预措施: Lidocaine (Drug)

Control group

Placebo Comparator

Patients will receive normal saline infusion for 6 hours

干预措施: Saline (Other)

结局指标

主要结局

The incidence of pruritis

时间窗: 24 hours postoperatively

The incidence of pruritis will be classifies as moderate (affecting a larger area, such as face and arms or face and anterior surface of thorax, but not disturbing the patient, and therefore not requiring treatment) , severe (extensive or generalized, often disturbing the patient and may need treatment)or very sever(disturbing the patient and treatment was indicated).

次要结局

  • The severity of pruritis(24 hours postoperatively)

研究者

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

Ayman Mohamady Eldemrdash

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine

Aswan University

研究点 (1)

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