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临床试验/CTRI/2025/06/088883
CTRI/2025/06/088883尚未招募1/2 期

Comparative Evaluation of Antimicrobial Efficacy of 5.25 percentage Sodium hypochlorite, 2 percentage Chlorhexidine, Ozonated Olive Oil and Diode laser In Irreversible Pulpitis Cases - A Randomized Controlled Trial

未提供1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年7月1日最近更新:

试验速览

阶段
1/2 期
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Reduction in microbial load by assessing the changes in bacterial colony forming units

研究概览

简要总结

The primary purpose of the study "Comparative Evaluation of Antimicrobial Efficacy of 5.25% Sodium Hypochlorite, 2% Chlorhexidine, Ozonated Olive Oil, and Diode Laser in Irreversible Pulpitis Cases - A Randomized Controlled Trial" is to compare the antimicrobial efficacy of four different treatment modalities in patients with irreversible pulpitis. This involves assessing and determining which of the treatments—5.25% sodium hypochlorite, 2% chlorhexidine, ozonated olive oil, or diode laser—provides the most effective microbial reduction in the affected pulp tissue, thereby aiding in the management and treatment of this dental condition.

The study hypothesizes that there will be significant differences in the antimicrobial efficacy of 5.25% sodium hypochlorite, 2% chlorhexidine, ozonated olive oil, and diode laser when used in the treatment of patients with irreversible pulpitis. Specifically, it posits that one or more of these treatments will demonstrate superior microbial reduction compared to the others

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients requiring endodontic treatment with irreversible pulpitis and single rooted teeth will be included in the trial.

排除标准

  • Medically / systemically compromised patients
  • Teeth where full working length cannot be reached
  • Teeth with periapical radiolucencies
  • Traumatic injuries
  • Teeth with developmental anomalies
  • Patients who do not give informed consent.

结局指标

主要结局

Reduction in microbial load by assessing the changes in bacterial colony forming units

时间窗: Baseline, post-operatively 12 hours, 24 hours

次要结局

  • Antimicrobial efficacy achieved(After 12 hours, 24 hours)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Akash Shailesh Thakare

Sharad Pawar Dental College

研究点 (1)

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