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临床试验/NCT04595721
NCT04595721撤回不适用

Comparison of Physical Versus Visual Distraction in the Reduction of Pain During Local Anesthesia

Virginia Commonwealth University0 个研究点开始时间: 2022年3月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Change in pain

研究概览

简要总结

The purpose of this study is to compare physical versus visual distractions to determine which technique reduces perceived pain better during local anesthesia injections.

详细描述

Before the local anesthesia injection, patients will be asked to give a preliminary VAS score based on what level of pain 0-10 they anticipate they will feel during the local anesthesia injection. Following the injection the participant will be asked to quantify the pain felt during the injection on a 0-10 Visual analog scale (VAS). The VAS scores will only be taken from the first injection of the appointment. Participants will be asked their gender, race, age, geographic location they spent most of their lives as well. Participants will be de-identified and randomly assigned a number that will be recorded along with their collected data on a two-factor, password protected web server. Information collected during this study may be used for further analysis and publication.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
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

  • Patients needing a dental procedure that requires a buccal infiltration with Septocaine 1:100,000 epinephrine (EPI) (Articaine hydrochloride 4% and EPI 1:100,000) or an inferior alveolar nerve block injection with 2% lidocaine with 1:100,000 epinephrine.
  • Adults greater than 18 years old.
  • Patients with limited English proficiency will be included only if their primary language is Spanish.

排除标准

  • Patients with a known or suspected allergy to anesthetic agent, sulfites, amide-type local anesthetic, or to any ingredient in anesthetic solutions will not be included.
  • Any patients taking medications affecting pain response on the day of the dental appointment.
  • Children younger than 18 years old.
  • Patients with limited English proficiency with a primary language other than Spanish

结局指标

主要结局

Change in pain

时间窗: Up to 30 minutes

Participants will be asked to rate their pain on a visual analog pain scale. The scale is rated from 0 (no pain) to 10 (pain as bad as it can be)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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