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临床试验/NCT00519207
NCT00519207已完成3 期

Evaluation of Topical Liposomal Lidocaine and Oral Sucrose for Treatment of Pain in Newborn Infants Undergoing Venipuncture: A Randomized Controlled Trial

The Hospital for Sick Children2 个研究点 分布在 1 个国家目标入组 330 人开始时间: 2007年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
330
试验地点
2
主要终点
Infant pain during venipuncture as assessed by facial grimacing response.

研究概览

简要总结

The objective of this study is to determine the relative efficacy of sucrose, liposomal lidocaine, and sucrose plus liposomal lidocaine, on reducing pain during venipuncture in newborn infants.

详细描述

Despite the fact that modern medical practice is greatly advanced, pain is inflicted on all Canadian newborn infants in the first days and months of life from blood tests, injections and cannulations designed to prevent, diagnose or manage medical conditions. Procedural pain in newborn infants is a significant burden to infants, their parents, healthcare workers, and society at large.

This study proposes a large randomized controlled trial to determine the optimal analgesic regimen for procedural pain using methods that can be easily implemented in clinical practice. We will study liposomal lidocaine cream and sucrose oral liquid, used alone, or together, to manage procedural pain. Liposomal lidocaine is a relatively new anaesthetic formulation ideally suited for young infants due to the established role of lidocaine in neonatal clinical medicine. Sucrose (sugar water) reduces pain responses and is promoted in consensus guidelines developed by pain experts. However, it is perceived by many front-line clinicians to be simply a comforting agent rather than a true analgesic. Studying liposomal lidocaine and sucrose together is important since the combination may prove superior to either agent alone, and may even prevent or abolish pain from clinical procedures.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
1 Day 至 7 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy newborn infants
  • ≥ 37 weeks gestational age.

排除标准

  • neonatal intensive care unit (NICU) admission
  • asphyxia, seizures
  • major birth defect (heart, brain, genetic syndrome)
  • circumcised during study
  • receiving analgesia/sedatives.

研究组 & 干预措施

1

Active Comparator

This group will receive lidocaine and sucrose placebo (water).

干预措施: Lidocaine (Drug)

2

Active Comparator

This group will receive lidocaine placebo and sucrose.

干预措施: 24% Sucrose Solution (Drug)

3

Active Comparator

This group will receive lidocaine and sucrose.

干预措施: Lidocaine (Drug)

3

Active Comparator

This group will receive lidocaine and sucrose.

干预措施: 24% Sucrose Solution (Drug)

结局指标

主要结局

Infant pain during venipuncture as assessed by facial grimacing response.

时间窗: During venipuncture

次要结局

  • Heart rate(During venipuncture)
  • Visual Analog Scale scores(During venipuncture)
  • Cry duration(During venipuncture)
  • Number of attempts until procedure completion(From first needle poke to completion)
  • Endomorphins-1,-2 levels(Before and 10 minutes after sucrose/sucrose placebo administration)
  • Procedure duration(From first needle poke to completion)
  • Lidocaine levels(5-15 minutes after the study cream is removed)

研究者

申办方类型
Other

研究点 (2)

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