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临床试验/CTRI/2020/09/027796
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.

研究者

发起方
Dr Namita Gandhi

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