Management of Post Endodontic Re-treatment Pain With Low-Level Laser Therapy
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
- 是
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
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
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
saranaz azari-marhabi
assistant professor
Shahid Beheshti University
