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临床试验/CTRI/2025/03/082942
CTRI/2025/03/082942已完成不适用

Comparative anesthetic efficacy evaluation of 2 percent Lignocaine, 3 percent Prilocaine and 4 percent Articaine during pulpectomy in mandibular primary molars - A parallel randomized control trail.

St Joseph Dental College1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2025年3月31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
96
试验地点
1
主要终点
Onset of anesthesia (evaluated using subjective and objective methods)

研究概览

简要总结

Pain during dental procedures is a significant source of fear and anxiety in children hence this study investigates the effectiveness of different local anaesthetics like 2 percent lignocaine, 3 percent prilocaine and 4 percent articaine in managing dental pain in children undergoing pulpectomy for primary mandibular molars.

The study compares the onset, duration, intraoperative pain, postoperative pain, and complications of these anaesthetics when administered via inferior alveolar nerve block (IANB) versus 4% articaine via infiltration in children aged 5–12 years.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Outcome Assessor Blinded

入排标准

年龄范围
5.00 Year(s) 至 12.00 Year(s)(—)
性别
All

入选标准

  • Healthy normal children ofAge group of5-12 years.
  • Children requiring pulpectomy for primary mandibular molars.

排除标准

  • Children whose parents/caregiver did not give the consent for the study.
  • Children with underlying systemic diseases.
  • Children with history of adverse reactions to anesthetic agents.
  • Children under medications that have adverse reactions to anesthetic agents.
  • Children with infection near injection site.

结局指标

主要结局

Onset of anesthesia (evaluated using subjective and objective methods)

时间窗: immediately after administration (ranges from seconds to minutes)

次要结局

  • duration of anesthesic action (evaluated using subjective & objective methods)(baseline (from onset to 4 hrs))
  • postoperative complications (identified using questionnaire)(24 hours post-treatment)

研究者

发起方
St Joseph Dental College
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Raparla Siva Teja

St. Joseph Dental College

研究点 (1)

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