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临床试验/NCT03562481
NCT03562481已完成4 期

Pilot Study: Comparison of Buffered 1% vs. Unbuffered 2% Lidocaine in Pediatric Subjects; Clinical Outcomes

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2018年7月24日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
26
试验地点
2
主要终点
Mean Pain Scores Following Injection

研究概览

简要总结

Local anesthesia is an integral part of clinical pediatric dental practice, but it has challenges. It can be uncomfortable for children, and the risk of adverse events limits how much is used. Some evidence suggests benefits of buffering local anesthetics including equal effect with less pain on injection. These findings have not been replicated and validated among pediatric populations, creating a gap in the knowledge base. To address this knowledge gap and contribute to the evidence base on safety and efficacy of local anesthesia in pediatric dentistry, this investigation proposes to compare the anesthetic effects of buffered 1% lidocaine with those of unbuffered 2%, among children.

The specific aims of this investigation are to determine differences between buffered 1% and unbuffered 2% lidocaine (both with 1:100,000 epinephrine) used for inferior alveolar nerve block (IAN) anesthesia, in the following domains:

  1. Pain experience on injection, time to onset following the administration, and time to recovery [subjective]
  2. Blood lidocaine levels 15 minutes following the administration and duration of pulpal anesthesia [objective]

Null Hypotheses:

  1. No difference exists in anesthetic effectiveness for pulpal anesthesia after intraoral IAN block between buffered 1% Lidocaine with 1:100,000 epinephrine as compared to unbuffered 2% Lidocaine with 1:100,000 epinephrine.
  2. No differences exist in peak blood lidocaine levels, pain on injection, time to lip numbness, and duration of anesthesia between the two drug formulations.

Randomized subjects will be injected orally for bottom jaw anesthesia, with 3cc of buffered 1% lidocaine (30mg) 1:100,000 epinephrine or 3cc unbuffered of 2% lidocaine (60mg) 1:100,000 epinephrine. The injectable volume of the buffered formulation will include 0.3cc of 8.4% sodium bicarbonate.

One faculty member in the Department of Pediatric Dentistry at the University of North Carolina (UNC) School of Dentistry will administer the drugs in the Pediatric Dentistry clinic. The same clinician will administer injection to the same subjects at both visits. Clinicians and subjects will not know which drug formulation is given at which appointment.

A clinician will measure the level of discomfort on injection, how long it takes for the lip to be numb, how long it takes for the first molar tooth in that area to be numb, how long it takes the local anesthetic to wear off, and how much of the anesthetic is in the blood.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
10 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age 10-12 years
  • American Society of Anesthesiologists (ASA) Class I (Healthy)
  • Body Weight: the Interquartile Range (IQR) 33-60Kg for subject ages
  • Have ability to speak and read English
  • Willingness to participate in two sessions
  • No history of adverse reaction to dental anesthetic
  • Have bilateral, disease/symptom-free mandibular first molars present

排除标准

  • Allergy to lidocaine class of anesthetic drugs
  • Local anesthetic drug use in past week
  • Current symptomatic teeth or oral mucosa
  • ASA II or above (including asthma)

结局指标

主要结局

Mean Pain Scores Following Injection

时间窗: Within 10 minutes of injection

Perceived pain on injection, self-reported verbally using a Likert scale from 1-10, with lower numbers corresponding to less pain (1 = "no pain," 10 = "worst pain imaginable"). Lower scores reflect a lesser degree of pain.

Mean Time to Lower Lip Numbness Following Injection

时间窗: Up to 30 minutes following injection

Time in minutes beginning immediately following injection to patient-reported lip numbness

Average Serum Lidocaine Concentration at 15 Minutes Post Injection

时间窗: One blood draw taken 15 minutes following injection

Blood Lidocaine Level (mcg/mL) as measured in 10cc venous blood, taken 15 minutes following injection. Blood assayed for serum lidocaine levels with a Sciex TripleTOF liquid chromatography- mass spectrometry (LC-MS) equipped with a C18 Hypersil (10mm x 2.1mm, 3.0μm).

Mean Time to Baseline Lip Sensation

时间窗: Within 24 hours following injection

Response in minutes from injection to when lip is no longer numb, as self reported by patient.

Number of Participants Who Respond to Cold Stimulus (Positive/Negative) Prior to Injection

时间窗: 5 minutes prior to injection

Response to experiencing sensation to cold stimulus on permanent molar tooth prior to injection

Number of Participants Who Respond to Cold Stimulus (Positive/Negative) 90 Minutes Following Injection

时间窗: 90 minutes following injection

Response to experiencing sensation to cold stimulus on permanent molar tooth 90 minutes following injection

Number of Participants Who Respond to Cold Stimulus (Positive/Negative) 120 Minutes Following Injection

时间窗: 120 minutes following injection

Response to experiencing sensation to cold stimulus on permanent molar tooth 120 minutes following injection

Number of Participants Who Respond to Cold Stimulus (Positive/Negative) 30 Minutes Following Injection

时间窗: 30 minutes following injection

Response to experiencing sensation to cold stimulus on permanent molar tooth 30 minutes following injection

Number of Participants Who Respond to Cold Stimulus (Positive/Negative) 60 Minutes Following Injection

时间窗: 60 minutes following injection

Response to experiencing sensation to cold stimulus on permanent molar tooth 60 minutes following injection

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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