Comparative Evaluation Of Anaesthetic Efficacy Of warm, Buffered And Conventional 2% Lignocaine For The Success Of Inferior Alveolar Nerve Block In Mandibular Primary Molars- A Randomized Clinical Controlled Trial.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- 1.Anaesthetic efficacy
研究概览
简要总结
This study is a randomized, double blinded, split mouth clinical trial, comparing the anaesthetic efficacy and patient’s pain reaction to warm lignocaine, buffered lignocaine and conventional 2% lignocaine during pulp therapy in primary mandibular molars. 50 patients were randomly divided into 2 groups and were given conventional lignocaine on one visit on one side and either buffered or warmed lignocaine on the other side during the next visit. The results showed that the pain on administration, mean onset of anaesthesia, pain during pulp therapy, the parameters of the SEM score and the duration of anaesthesia were all significantly lower for the buffered and warmed solutions compared to the conventional solution. However there was no significant difference on comparing the warmed and buffered groups with each other. Thus it can be concluded that modifying local anaesthesia by either buffering it or warming it can be beneficial in reducing the pain on injection and during pulp therapy, especially in children.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 6.00 Year(s) 至 12.00 Year(s)(—)
- 性别
- All
入选标准
- •1.patients having deep dentinal caries extending through half the dentinal depth wrt 74, 75, 84, 85
- •patients complaining of mild to moderate pain.
- •3.teeth with vital pulp 4.children with frankl behaviour rating of 3 or 4 5.patients whose parents/guardians give consent 6.subjects should be free of systemic disease 7.the agreement to comply with study visits and procedures.
排除标准
- •1.patients who are physically or medically compromised/ systemic disease 2.patients with allergies to local anaesthetics, sulphites or sodium bicarbonate 3.patients on any medication 4.presence of abscess or sinus openings at the site of injection or at the tooth involved.
- •5.children with frankl behaviour rating of 1 or 2.
结局指标
主要结局
1.Anaesthetic efficacy
时间窗: 3-5 hours
2.The patient’s pain reaction
时间窗: 3-5 hours
次要结局
- 1.Pain during administration of anaesthesia(2.Onset of anaesthesia)
