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临床试验/CTRI/2025/10/095699
CTRI/2025/10/095699尚未招募2/3 期

Assessment of anesthetic efficacy of Buccal infiltration with 4 percent Artcaine , 0.5 percent Bupivacaine and 2 percent Lidocaine Inferior Alveolar Nerve Block in Vital Pulp Therapy A Randomized Clinical Trial

Dr Hetal Joshi1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年10月20日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
The primary outcome of the study is satisfactory anesthetic efficacy with 4% Articaine , 0.5% Bupivacaine and IANB with 2% lignocaine

研究概览

简要总结

The study compares the anesthetic efficacy of 4 percent articaine and 0 point 5 percent bupivacaine buccal infiltration with 2 percent lidocaine inferior alveolar nerve block in children aged 12 to 16 years requiring vital pulp therapy. Ninety children were randomly divided into three groups. Pain was assessed using heft parker visual analog scale  pre operatively and post operatively ,sound eye motor scores will be record during treatment and facial image scale post operatively . Post operative complications will be record after 24 hours at site of injection . The aim is to compare and evaluate 3 different local anesthtic is better  for pain control in pediatric dentistry.

研究设计

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

入排标准

年龄范围
12.00 Year(s) 至 16.00 Year(s)(—)
性别
All

入选标准

  • Permanent first and second mandibular molars indicated for vital pulp therapy will be selected based on clinical and radiographic screening.
  • Hot tooth 3)Age group 12-16 years 4)Pulp involved vital tooth 5)ASA I.

排除标准

  • Teeth with abscess , fistula, With swelling 2)RC treated 3)Periapical lesion 4)Furcation involved 5)Patient allergic to LA 6)Systemically compromised and patients with history of drug allergy ASA II ASA III 7)Children / Guardian who are not willing.

结局指标

主要结局

The primary outcome of the study is satisfactory anesthetic efficacy with 4% Articaine , 0.5% Bupivacaine and IANB with 2% lignocaine

时间窗: Pain is evaluated peroperative before starting procedure by patient heft parker visual analog scale HP VAS , during treatment Sound eye motor SEM will be recorded on caries excavation reaching deep dentine and /or pulp , after completion of procedure patient will be asked to record facial image scale ,heft parker visual analog scale study will be conducted in single visit appointment of patient assessment will be done intraoperatively and Postoperatively within one hour of time period

次要结局

  • post operative complication at site of injection(after 24 hours through telephonic communication)

研究者

发起方
Dr Hetal Joshi
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Hetal Joshi

JMFS ACPM DENTAL COLLEGE SAKRI ROAD DHULE

研究点 (1)

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