Needle-free Dental Anesthesia: a Pilot Split-mouth Cross-over Randomized Clinical Trial.
试验速览
- 阶段
- 不适用
- 状态
- 暂停
- 发起方
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Efficacy of dental pulp anesthesia
研究概览
简要总结
Many patients experience pain and anxiety from traditional needle anesthesia and may avoid necessary dental treatments. The needle-free liquid jet injection(NFLJI) could solve these problems. NFLJI delivers drug solutions by creating a micro-thin pressure liquid jet to penetrate the skin and disperse in the soft tissue. It has many advantages like eliminating injection pain, needle phobia and needle disposal. However, anesthesia techniques in dentistry were all developed for needle injection, and they are not very effective for NFLJI. Moreover, clinical trials of dental anesthesia using NFLJI have shown inconsistent efficacy.
In this study, we aim to compare the clinical efficacy between NFLJI and needle dental anesthesia in pilot split-mouth cross-over randomized clinical trials, assess the feasibility to conduct such trial on a larger scale.
Participants will be assigned to one of the following four groups: 1. Infiltration on a maxillary lateral incisor,2. Inferior alveolar nerve block, 3.Mental nerve block, 4. Infraorbital nerve block. Each participant will receive one injection with a needle and another one with NFLJI randomly at the same appointment. A washout period of 1 hour between two procedures for participants' to forget the previous experience. Needle injection will be performed according to clinical standards. NFLJI will be performed according to a guideline developed in our research group. Participants will stay in the clinic until the anesthesia effect disappear and be followed for one week.
The primary outcome is the efficacy and effect of two anesthesia interventions. The secondary outcome is the pain and anxiety visual analogue scale before and during injection, taste preference, and complications. Additionally, patients' overall feelings for two interventions as well as any barriers to conducting such a trial will be recorded.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Double (Investigator, Outcomes Assessor)
盲法说明
Each participant receive two anesthesia methods randomly. Total 8 arms, 4 groups, each group will recruit 6 participants. Incase of drop out, a total of 30 participant will be enrolled.
入排标准
- 年龄范围
- 18 Years 至 35 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •age between 18-35 years-old
- •fluent in English
- •cooperate
排除标准
- •has a history of chronic pain,
- •has a systematic disease,
- •has root canal therapy at the upper lateral incisor/lower posterior teeth region.
结局指标
主要结局
Efficacy of dental pulp anesthesia
时间窗: 10 minutes after injection.
The number of sucessful dental pulp anesthesia cases over total number of participants in the group.
Time to termination of anesthesia
时间窗: 3 hours after injection
Time to termination of anesthesia feeling, measured by a simple pinch test using a periodontal probe
Dental pulp anesthesia
时间窗: 10 minutes after injection.
Dental pulp anesthesia result is measured by an electric pulp test(EPT), successful anesthesia for dental pulp exhibits an EPT at 80.
Time to initiation of anesthesia
时间窗: 1 minute after injection
Time to initiation of anesthesia feeling, measured by a simple pinch test using a periodontal probe
次要结局
- Taste preference(1 minute after the injection)
- Incidence of adverse effect [safety](10 seconds after injection.)
- Pain level during injection(10 seconds after the injection)
- Baseline anxiety level(1 minute before injection)
- Baseline pain level(1 minute before injection)
- Anxiety level during injection(10 seconds after the injection.)
- Incidence of adverse effect during follow-up period[safety](up to 7 days)
研究者
Faleh Tamimi
Associate Professor, Accociate Dean
McGill University Health Centre/Research Institute of the McGill University Health Centre
