CTRI/2020/09/027796已完成未知
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
Dr Namita Gandhi0 个研究点目标入组 252 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 252
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Both male and female patients between 18-60 years of age will be included in the study.
- •2. Patients diagnosed with symptomatic irreversible pulpitis with or without apical periodontitis. 34
- •3. Patient should have actively experienced moderate to severe pain pre operatively on VAS scale.32
- •4. 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.
- •5. 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.
- •2. Pregnant and lactating patients will be excluded from study.
- •3. Patients taking any analgesics, antibiotics, sedatives, and antianxiety drugs on regular basis or before 24 hrs. of treatment will be excluded.
- •4. Patient having history of significant medical condition will be excluded from study.
- •5. Patient having necrosed tooth with sinus tracts/local gum swelling around the affected tooth.
- •6. Patients with severe periodontitis and poor oral hygiene.
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