To evaluate the success rate of 0.5 percent Bupivacaine v/s 4 percent Articaine as anesthetic agents in teeth with Symptomatic Irreversible Pulpitis
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Pain Control and Effectivity with Bupivacaine and Articaine
研究概览
简要总结
Following the clinical examination and diagnosis of symptomatic irreversible pulpitis, patients will be randomly assigned to one of two groups. The procedure will be explained to the patients, and informed consent will be obtained. Anesthesia will be administered by a postgraduate student, followed by root canal treatment performed by another postgraduate student. Pain evaluation will be done before the administration of local anesthesia, 15 minutes post-administration, and during access cavity preparation to assess the effectiveness and success of the local anesthesia using various techniques.
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 Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 55.00 Year(s)（—）
- 性别
- All
入选标准
- •Systemically healthy patients.
- •Mature permanent mandibular posteriors with symptomatic irreversible pulpitis with no periapical radiolucency Teeth having sufficient tooth structure for adequate isolation.
- •A vital coronal pulp on access opening No history of previous endodontic therapy.
- •No history of trauma to the involved tooth.
排除标准
- 未提供
结局指标
主要结局
Pain Control and Effectivity with Bupivacaine and Articaine
时间窗: Before administration of local anesthesia, 15 minutes after administration of anesthesia, during instrumentation
次要结局
未报告次要终点
研究者
NIMISHA JAIN
SGT DENTAL COLLEGE HOSPITAL AND RESEARCH INSTITUTE,SGT UNIVERSITY