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Efficacy of Pre-cooling and Sweet-tasting Solution on Pain Related to Local Anesthesia Injection in Children

2026年9月16日 更新者:Nada Mohammed Farouk、British University In Egypt

Efficacy of Pre-cooling and Sweet-tasting Solution on Pain Related to Local Anesthesia Injection in Children: A Randomized Control Trial

The study aims to determine whether pre-cooling and sweet-tasting solutions, alone or combined with topical anesthesia, provide better pain control during dental local anesthesia in children.

It has two phases:

Phase 1: Identify the children's preferred sweet-tasting solution among xylitol, monk fruit, erythritol, and honey.

Phase 2: A randomized controlled trial comparing 7 groups involving pre-cooling, sweet solution, topical anesthesia, and their combinations.

The primary outcome is pain measured by VAS, while secondary outcomes include SEM behavioral response, heart rate, and oxygen saturation. The planned sample is 220 children.

研究概览

研究类型

介入性

注册 (估计的)

224

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • El Sherouk
      • Cairo、El Sherouk、埃及
        • 招聘中
        • Faculty of Dentistry, British University in Egypt
        • 接触:
        • 接触:
          • Ola A Abd El-geleel, Associate Professor
          • 电话号码:+21006086830
          • 邮箱:ola@dent.asu.edu.eg
        • 副研究员:
          • Noha S Kabil, professor
        • 首席研究员:
          • Nada M Farouk, bachelors degree
        • 副研究员:
          • Ola A Abd El-Geleel, associate professor

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

7年 至 11年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age group 7-11 years
  2. Patients requiring infiltration anesthesia to fulfill dental therapeutic needs
  3. Frankl behavior scale 3 and 4

Exclusion Criteria:

  1. Failure to provide assent or consent
  2. Allergy from local anesthetic solution
  3. Systemic diseases such as diabetes that could affect pain perception
  4. History of abscess or fistula at site of injection

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Precooling group

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

实验性的:Precooling + topical anaesthesia group

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

实验性的:Precooling + sweet tasting solution group

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

实验性的:Precooling + sweet tasting solution + topical anaesthesia

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

实验性的:Sweet tasting solution group

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

实验性的:Sweet tasting solution + topical anaesthesia group

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

有源比较器:Topical anaesthesia group

The intervention consists of pre-cooling and/or a sweet-tasting solution, used alone or in combination with topical local anesthesia, before administration of the dental local anesthetic injection.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Visual Analog Scale (VAS)
大体时间:Immediately after intervention

Pain Intensity assessed by visual analogue scale

Immediately after intervention

次要结果测量

结果测量
措施说明
大体时间
Phase 1 outcome
大体时间:After intervention

The preferred sweet tasting solution based on number of patients

After intervention
Heart Rate
大体时间:Heart rate (beats per minute) measured immediately before needle insertion (baseline) and during needle injection and after needle injection

Heart rate (beats per minute) measured immediately before needle insertion (baseline) and the maximum heart rate recorded during needle injection and after needle injection

Heart rate (beats per minute) measured immediately before needle insertion (baseline) and during needle injection and after needle injection
Sound, eye and motor scale (SEM) scale
大体时间:During needle injection

Behavioral pain response during local anesthetic injection assessed using the Sound, Eye, and Motor (SEM) Scale. Sound, eye, and motor responses are each scored from 1 to 4, with 1 indicating comfort and 4 indicating a painful response. The three component scores are summed to obtain a total SEM score ranging from 3 to 12, with higher scores indicating greater behavioral response to pain.

During needle injection
Oxygen saturation
大体时间:Immediately before needle injection (baseline), during needle injection, and immediately after completion of injection. Recorded as percentage

Peripheral oxygen saturation (SpO₂) will be measured using a pulse oximeter and recorded as a percentage at three time points: immediately before local anesthetic needle injection (baseline), during needle injection, and immediately after completion of the injection.

Immediately before needle injection (baseline), during needle injection, and immediately after completion of injection. Recorded as percentage

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年10月6日

初级完成 (估计的)

2027年1月1日

研究完成 (估计的)

2027年4月1日

研究注册日期

首次提交

2026年9月7日

首先提交符合 QC 标准的

2026年9月16日

首次发布 (实际的)

2026年9月22日

研究记录更新

最后更新发布 (实际的)

2026年9月22日

上次提交的符合 QC 标准的更新

2026年9月16日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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