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Low-Level Laser Therapy: A Noninvasive Method of Relieving Postactivation Orthodontic Pain—A Randomized Controlled Clinical Trial

机译:低水平激光治疗:缓解激活后正畸疼痛的非侵入性方法—随机对照临床试验

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Introduction: Pain is an unavoidable squeal of orthodontic treatment and it is known to decrease patient compliance and eventually affects treatment results. Numerous methods are available in literature to manage orthodontic pain after activation but they have their own limitations. This has led to exploring further options for management of pain. Aim: The aim of this study was to evaluate the effectiveness of low-level laser therapy (LLLT) in alleviating orthodontic pain after activation. Materials and Methods: 20 subjects were randomly divided into an experimental and a control group. Each participant was given a retraction force of 200 gm/cmsup2/sup/side. Subjects in the experimental group were exposed to low-level laser light at 980 nm and those in the control group were exposed to red LED light as placebo. The pain perceived after 0 hour, 1 hour, 3 hours, 48 hours, and 1 week of activation was recorded by patient using Visual Analog Scale. Statistical analysis was done using Mann–Whitney test. Results: Results of the study showed that pain experienced by the subjects after orthodontic activation was higher in experimental group at Tsub0/sub than in placebo group. At Tsub1/sub, Tsub2/sub, Tsub4/sub, and Tsub5/sub, the pain experienced by the subjects was less in the experimental group compared to the placebo group. Pain experienced by the subjects in the experimental group at Tsub3/sub was significantly less as compared to those in the placebo group. Conclusion: A single dose of LLLT at 980nm, 2.5 W/cmsup2/sup, and 600 J is effective in relieving orthodontic pain after activation.
机译:简介:疼痛是正畸治疗的必然结果,众所周知,疼痛会降低患者的依从性并最终影响治疗效果。文献中提供了许多方法来控制激活后的正畸疼痛,但是它们有其​​自身的局限性。这导致探索更多的疼痛控制选择。目的:本研究的目的是评估低水平激光疗法(LLLT)缓解激活后正畸疼痛的有效性。材料与方法:将20名受试者随机分为实验组和对照组。每位参与者的回缩力为200 gm / cm 2 /面。实验组的受试者暴露于980 nm的弱激光下,对照组的受试者作为安慰剂暴露于红色LED灯下。患者使用Visual Analog Scale记录激活后0小时,1小时,3小时,48小时和1周后感觉到的疼痛。使用Mann-Whitney检验进行统计分析。结果:研究结果表明,在正畸激活后受试者在T 0 处经历的疼痛高于安慰剂组。在T 1 ,T 2 ,T 4 和T 5 时,受试者经历的疼痛减轻实验组与安慰剂组相比。与安慰剂组相比,实验组的受试者在T 3 所经历的疼痛明显更少。结论:980nm,2.5 W / cm 2 和600 J的单剂量LLLT可以有效缓解激活后的正畸疼痛。

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