跳至主要内容
临床试验/CTRI/2024/12/078736
CTRI/2024/12/078736已完成Phase 3 4

Comparative evaluation of the efficacy of supplemental local anesthesia using temperature variation along with pharmacological agents for irreversible pulpitis: a randomized controlled trial

Aakash Gupta1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年1月10日最近更新:

试验速览

阶段
Phase 3 4
状态
已完成
发起方
入组人数
120
试验地点
1
主要终点
effect of various agents as supplemental anesthesia on onset and duration of anesthesia for patients with symptomatic irreversible pulpitis

研究概览

简要总结

This study is a randomized, double blind, parallel group, multi-center trial comparing the efficacy of various pharmacological agents such as 1ml/4mg of dexamethasone, 1 mL/30 mg of ketorolac tromethamine, 1ml/50mg of tramadol when used as a supplemental local anesthetic agent along with temperature variation of local anesthesia (2% lignocaine with 1:200000 adrenaline) at different temperature such as cold LA at 4degree celsius and warm LA at 37 degree celsius used for supplemental buccal infiltration along with conventional inferior alveolar nerve block(2% lignocaine with 1:200000 adrenaline).  Pain Numerical scale is used for noting the response obtained from patients.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Teeth with symptomatic irreversible pulpitis Teeth with normal tooth anatomy Class I or II medical history (American Society of Anesthesiologists).

排除标准

  • Allergic to local anesthesia Periodontally compromised teeth.
  • Teeth with vertical fracture.

结局指标

主要结局

effect of various agents as supplemental anesthesia on onset and duration of anesthesia for patients with symptomatic irreversible pulpitis

时间窗: 3 minutes after injection local infiltration before starting treatment and during the procedure

次要结局

  • any associated side effect(duration of supplemental local anesthesia)
  • patient pain levels assessed before & after the procedure using numeric pain rating scale(pain rating scale before & after the completion of procedure)

研究者

发起方
Aakash Gupta
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Aakash Gupta

AIIMS, Bathinda

研究点 (1)

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