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临床试验/NCT07439614
NCT07439614招募中不适用

Comparison of Different Root Canal Disinfection Protocols for Bacterial Reduction in Teeth With Apical Periodontitis Using Two Analytical Microbiological Methods: a Randomized Clinical Study

State University of New York at Buffalo1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1

研究概览

简要总结

Evaluate and compare the disinfecting efficacy of two supplementary antimicrobial protocols in teeth with apical periodontitis

详细描述

This study aims to evaluate and compare the disinfecting efficacy of two supplementary antimicrobial protocols in teeth with apical periodontitis: Er,Cr:YSGG laser activated irrigation and ultrasonic activation using a piezoelectric ultrasonic device (Dentsply International Inc., York, PA, USA) and Irrisafe tip (Satelec/Acteon, Merignac, France), comparing the detection of bacteria before and after instrumentation.

Secondary aims are to assess presence of bacteria before and after chemomechanical preparation using two microbiological methods:

  • ATP level analysis using the Endocator device
  • Quantitative PCR (qPCR) for total bacterial quantification.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients able to give informed consent and willing/able to comply with study procedures and follow-up.
  • Molar teeth indicated for endodontic treatment.
  • Teeth with intact pulp-chamber walls (no extensive coronal destruction).
  • Necrotic pulp confirmed by pulp testing.
  • Clinical and radiographic evidence of asymptomatic apical periodontitis.

排除标准

  • Immature teeth
  • Teeth with calcified or obliterated canals
  • Teeth with extensive coronal destruction
  • Teeth with previous endodontic treatment
  • Symptomatic apical periodontitis
  • Teeth with periodontal pockets greater than 4 mm
  • Patients who have received systemic antibiotics in the last 3 months
  • Patients with a history of diabetes or immune impairment
  • Pregnant patients

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Stephen M. Lyon, D.D.S

Principal Investigator

State University of New York at Buffalo

研究点 (1)

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