A Comparative Evaluation of Efficacy of Inferior Alveolar Nerve Block with Conventional, Pre-heated and Buffered 2% Lignocaine in Patients with Symptomatic Irreversible Pulpitis- A Randomized Clinical Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 180
- 试验地点
- 1
- 主要终点
- 1.To evaluate the efficacy of preheated local anaesthetic ie. 2% Lignocaine in patient with symptomatic irreversible pulpitis on giving inferior alveolar nerve block checked on VAS scale. 2.To evaluate efficacy of buffered local anaesthetic ie.2% Lignocaine on VAS scale.3.To evaluate efficacy of conventional local anaesthetic ie. 2% Lignocaine checked on VAS scale.4.To compare the efficacy of conventional, pre-heated and buffered local anesthetics ie. 2% Lignocaine checked on VAS scale.
研究概览
简要总结
.To compare the efficacy of conventional, pre-heated and buffered local anesthetics ie. 2% Lignocaine in patients with symptomatic irreversible pulpitis on giving inferior alveolar nerve block checked on VAS scale.
To compare pain on injection between conventional, pre-heated and buffered local anaesthetic ie. 2% Lignocaine in patients with symptomatic irreversible pulpitis on Administrating inferior alveolar nerve block checked on VAS scale on mandibular posterior teeth.
The main purpose of study is to evaluate the pain pre and post operatively following an Endodontic access cavity preparation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Both male and female patients between 18-60 years of age will be included in the study.
- •Patients diagnosed with symptomatic irreversible pulpitis with or without apical periodontitis.
- •Patient should have actively experienced moderate to severe pain pre operatively on VAS scale.32
- •A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.
- •Patients diagnosed with symptomatic irreversible pulpitis in mandibular molar teeth will be included in study.
排除标准
- •Patients allergic to local anesthetics or known allergy to sodium bicarbonates will be excluded from study.
- •Pregnant and lactating patients will be excluded from study.
- •Patients taking any analgesics, antibiotics, sedatives, and antianxiety drugs on regular basis or before 24 hrs.
- •of treatment will be excluded.
- •Patient having history of significant medical condition will be excluded from study.
- •Patient having necrosed tooth with sinus tracts/local gum swelling around the affected tooth.
- •Patients with severe periodontitis and poor oral hygiene.
结局指标
主要结局
1.To evaluate the efficacy of preheated local anaesthetic ie. 2% Lignocaine in patient with symptomatic irreversible pulpitis on giving inferior alveolar nerve block checked on VAS scale. 2.To evaluate efficacy of buffered local anaesthetic ie.2% Lignocaine on VAS scale.3.To evaluate efficacy of conventional local anaesthetic ie. 2% Lignocaine checked on VAS scale.4.To compare the efficacy of conventional, pre-heated and buffered local anesthetics ie. 2% Lignocaine checked on VAS scale.
时间窗: pre and post operatively
次要结局
- To compare pain on injection between conventional, pre-heated and buffered local anaesthetic ie. 2% Lignocaine in patients with symptomatic irreversible pulpitis on Administrating inferior alveolar nerve block checked on VAS scale on mandibular posterior teeth.(after inferior alveolar nerve block)