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临床试验/CTRI/2022/10/046857
CTRI/2022/10/046857已完成1 期

A Comparative Evaluation of the Efficacy of ‘OPG- assisted Inferior Alveolar Nerve Block’ Technique with the Conventional Technique in Permanent Mandibular Molars with Symptomatic Irreversible Pulpitis : A Randomized Double-blinded Clinical Study ?

Dr DIKSHIT SOLANKI0 个研究点目标入组 34 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
34

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

  • 1.Systemically healthy Patients (ASA 1 & 2) between age group of 18-60 years will be included in the study.
  • 2.Patients with pre-operative moderate to severe pain i.e. VAS score of 4 and above in mandibular molars will be included in the study.
  • 3.Patient having fully erupted last tooth in the mandibular arch upto the level of occlusion will be included in the study.
  • 4.Patients showing hyper response to cold and electric pulp testing (EPT) will be included in the study.
  • 5.Patients with symptomatic irreversible pulpitis with/without symptomatic apical periodontitis (only vital teeth) will be included in the study.
  • 6.Patients requiring treatment of multiple teeth along with the concerned tooth will be included in the study.
  • 7.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.

排除标准

  • 1.Asymptomatic Non-Vital Teeth with/without periapical radiolucency be it abscess or granuloma etc will be excluded.
  • 2.Patients showing active sites of pathosis in the injection area.
  • 3.Medically compromised patients will be excluded.
  • 4.Teeth with completely obliterated canals will be excluded
  • 5.Teeth with open apex, root resorption or complex root canal anatomy will be excluded.
  • 6.Teeth with vertical root fractures, cracks, etc will be excluded.
  • 7.Patient with deep periodontal disease or endo-perio lesion with periodontal phase dominant will be excluded.
  • 8.Patients with restricted mouth opening will be excluded.
  • 9.Pregnant and lactating women will be excluded.
  • 10.Patients using medications that might affect the anesthetic assessment will be excluded.
  • 11.Patients allergic to lidocaine and/or adrenaline will be excluded.

研究者

发起方
Dr DIKSHIT SOLANKI

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