Comparative Evaluation of Pain Perception and Anxiety of patient using different techniques of Inferior alveolar nerve block in mandibular teeth with symptomatic irreversible pulpitis using a newly introduced device & its components and the conventional syringe technique A randomized clinical study - NI

Dikshit Mahendra Solanki0 个研究点目标入组 60 人开始时间: 待定最近更新: 2024年4月29日

试验速览

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•1.Patients with Pre-operative moderate to severe pain i.e. VAS score of 4 and above in teeth with symptomatic irreversible pulpitis will be included in the study.
•2.Patients not having prior experience of administration of Local anesthesia will be included in the study.
•3.Patients showing Delayed response to cold and electric pulp testing (EPT) will be included in the study.
•4.Patients with symptomatic irreversible pulpitis with/without symptomatic apical periodontitis (only vital teeth) will be included in the study.
•5. Patients without any inflammation or trauma on the external surface of concerned cheek will be included in the study.
•6.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.

•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.

发起方

Dikshit Mahendra Solanki