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临床试验/NCT06862570
NCT06862570已完成2 期

Assessment of Local Anaesthesia Effectiveness Using Electric Pulp Tester in Symptomatic Irreversible Pulpitis Using 2% Lignocaine and 4% Articaine As Supplemental Anaesthetic Agents: an in Vivo Comparison

28 Military Dental Centre Lahore1 个研究点 分布在 1 个国家目标入组 123 人开始时间: 2022年12月19日最近更新:
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
123
试验地点
1
主要终点
Assessment of Local anaesthsia effectiveness in symptomatic irreversible pulpitis after afailed inferior alveolar nerve block using supplemental buccal infiltration

研究概览

简要总结

This study aims to evaluate the comparative efficacy of two different local anaesthetic agents for supplemental buccal infiltration after a failed inferior alveolar nerve block in achieving profound pulpal anaesthesia for symptomatic irreversible pulpitis using 2% lignocaine and 4% articaine with vasoconstrictor epinephrine.

Alternate hypothesis:

There is a mean difference in local anaesthesia effectiveness of 2% lignocaine and 4% articaine containing epinephrine when used for buccal infiltration in pulpectomy of symptomatic irreversible pulpitis of mandibular posterior teeth after a failed inferior alveolar nerve block

详细描述

Patients diagnosed with symptomatic irreversible pulpitis are included in this study. Teeth will be divided into two groups after a failed inferior alveolar nerve block using 2% lignocaine containing 1:100,000 epinephrine. A sample size of 123, with the first group consisting of 62 patients, 2 cartridges of 32mg of 2% lignocaine with 1:100,000 epinephrine will be used for supplemental buccal infiltration. In group 2 of 61 patients, 40mg of 4% articaine with 1:100,000 epinephrine will be used. During the root canal treatment, a subjective assessment of lip anesthesia is recorded. An electric pulp tester is used for the evaluation of the presence or absence of pulpal anesthesia. A verbal analogue scale is also used to evaluate the presence or absence of pain.

After taking a brief history, informed consent will be taken. A rubber dam will be used. Electric pulp tester will be used on the control contralateral tooth, the experimental tooth preoperatively; after giving nerve block and achieving Lip numbness, the experimental tooth will again be evaluated with Electric pulp tester. An access cavity will be made. If there is still no pulpal anesthesia, supplemental anesthesia will be administered and Electric pulp tester will be used again.

A questionnaire containing a numerical rating scale will be given to each patient to record the intensity of pain felt after giving supplemental anesthesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with ages ranging from 18-to 55 years
  • Male/ Female
  • Mandibular posterior teeth with symptomatic irreversible pulpitis
  • Ability to understand the use of the pain scale
  • Patients with adequate oral hygiene and willing to participate in the study

排除标准

  • Any type of medication consumed before treatment
  • Patients who do not show profound lip numbness after giving inferior alveolar block
  • Periapical pathologies ( periapical abscess, sinus tract, periapical cyst, pulpal necrosis)
  • External resorption
  • Unfavorable location of the tooth, internal ankylosis, trismus, severe tooth malposition.

研究组 & 干预措施

2% LIGNOCAINE WITH EPINEPHRINE

Experimental

1.8 ml of 2% Lignocaine with 1:100,000 epinephrine (36 mg/ml Lignocaine HCL, epinephrine bitartrate 0.0324 mg/ml)

干预措施: 2% lignocaine with epinephrine 1.8 ml(36mg/ml lignocaine HCL, epinephrine bitartrate 0.0324mg/ml) (Drug)

4% ARTICAINE WITH EPINEPHRINE

Experimental

1.7 ml of 4% Articaine with 1:100,000 epinephrine (40mg/ml Articaine HCL, epinephrine bitartrate 0.018mg/ml)

干预措施: 4% Articaine with epinephrine 1.7 ml (40mg/ml Articaine HCL, epinephrine bitartrate 0.018 mg/ml) (Drug)

结局指标

主要结局

Assessment of Local anaesthsia effectiveness in symptomatic irreversible pulpitis after afailed inferior alveolar nerve block using supplemental buccal infiltration

时间窗: 5-10 minutes after administrating supplemental buccal infiltration

Numeric Rating scale to assess absence or presence of pain after supplemental buccal infiltration

次要结局

未报告次要终点

研究者

发起方
28 Military Dental Centre Lahore
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Zahra Zubair

Dr Zahra Zubair

28 Military Dental Centre Lahore

研究点 (1)

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