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临床试验/NCT03023761
NCT03023761Unknown不适用

Management of Post Endodontic Re-treatment Pain With Low-Level Laser Therapy

Shahid Beheshti University1 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2017年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
61
试验地点
1
主要终点
reduction of pain after low level laser irradiation

研究概览

简要总结

In this clinical trial investigators aimed to evaluate Post endodontic re-treatment pain after irradiation of low level laser therapy

详细描述

In this clinical trial, 61 patients requiring endodontic retreatments in the posterior teeth were selected. A single visit Endodontic retreatment was done. After biomechanical preparation, Low Level Laser was irradiated to the buccal and lingual mucosa overlying the apices of the target tooth in the experimental group. In the control group patients received placebo laser to eliminate the probable psychological effects of laser. Laser irradiation was done with a single dose of 808 nm wavelength (Whitening Lase II- Laser DMC, Samsung, Korea) with 100 mw power, and dose of 70 J/cm2 for 80 seconds. Pain severity was recorded before the treatment, immediately after the treatment and 4, 8, 12, 24 and 48 hours after the treatment by visual analogue scale (VAS). The pain scores were statistically analyzed by chi-square test between two groups. The effects of different variables on the post-operative pain experience were also studied by means of Logistic regression.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • patients requiring endodontic retreatments in the posterior teeth

排除标准

  • systemic diseases psychologic disorders

研究组 & 干预措施

low level laser

Active Comparator

A single visit Endodontic retreatment was done. After biomechanical preparation, Low Level Laser was irradiated to the buccal and lingual mucosa overlying the apices of the target tooth in the experimental group

干预措施: low level laser (Device)

laser sham

Placebo Comparator

In the control group patients received placebo laser to eliminate the probable psychological effects of laser.

干预措施: laser sham (Device)

结局指标

主要结局

reduction of pain after low level laser irradiation

时间窗: baseline and 4, 8, 12, 24 and 48 hours after the treatment

次要结局

未报告次要终点

研究者

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

saranaz azari-marhabi

assistant professor

Shahid Beheshti University

研究点 (1)

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