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临床试验/CTRI/2017/03/008204
CTRI/2017/03/008204已完成不适用

Evaluation of different type of anesthetic techniques on anesthetic success rates in mandibular premolars with symptomatic irreversible pulpitis

Self funded1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2015年1月10日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
ability to undertake pulp access and canal instrumentation with no or mild pain

研究概览

简要总结

The inferior alveolar nerve block (IANB) is the most commonly used technique for achieving pulpal anesthesia for posterior mandibular endodontic procedures. In mandibular premolars, buccal infiltration provides adequate anesthesia. The purpose of this prospective randomized study is to compare IANB and buccal infiltration on anesthetic success rates. Adult volunteer subjects will be selected from dental OPD and included in this prospective, randomized study. The success is defined as the ability to undertake pulp access and canal instrumentation with no or mild pain (Heft-Parker VAS score<55mm). The subjects should be actively experiencing pain and in good health, and none will be taking any medication that would alter pain perception, as determined by oral questioning and written questionnaire. An informed written consent will be obtained from each subject. The patients will be randomly allocated to the treatment groups. Patients will receive standard inferior alveolar nerve block or buccal infiltrations. A conventional access opening will be initiated after isolation with a rubber dam. Patients will be instructed to raise their hand if any pain was felt during the procedure. In case of pain during the treatment, the procedure will be stopped, and patients asked to rate the pain on HP VAS. Success will be defined as no pain or weak/mild pain during endodontic access preparation and instrumentation .

研究设计

研究类型
Interventional
分配方式
Stratified block randomization
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • The subjects should be actively experiencing pain and in good health, and none will be taking any medication that would alter pain perception.

排除标准

  • Patients with underlying systemic diseases.

结局指标

主要结局

ability to undertake pulp access and canal instrumentation with no or mild pain

时间窗: The primary outcome shall be assessed after the administration of local anesthetic solution and during the procedure. If the patient experiences pain during any point of the procedure the anesthesia will be considered as failure.

次要结局

  • ability to undertake pulp access and canal instrumentation with no or mild pain(It will assessed at the end of the endodontic treatment.)

研究者

发起方
Self funded
申办方类型
Government medical college

研究点 (1)

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