首页> 外文期刊>American Journal of Orthodontics and Dentofacial Orthopedics >Impact of extracorporeal shock-wave therapy on the stability of temporary anchorage devices in adults: A single-center, randomized, placebo-controlled clinical trial
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Impact of extracorporeal shock-wave therapy on the stability of temporary anchorage devices in adults: A single-center, randomized, placebo-controlled clinical trial

机译:体外冲击波治疗对成人临时固定装置稳定性的影响:一项单中心,随机,安慰剂对照的临床试验

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Introduction: In this randomized, placebo-controlled clinical trial, we investigated the effect of noninvasive extracorporeal shock waves on the stability of temporary anchorage devices (TADs) under orthodontic loading. Methods: Thirty adult orthodontic patients of the Bernhard Gottlieb University Clinic in Vienna, Austria, were enrolled in this clinical trial and allocated by block randomization (size, 4) in a 1: 1 ratio to either the treatment or the placebo group. Randomization was performed with software, and the allocations were concealed in sealed envelopes. Eligibility criteria included healthy adult patients with mesially directed orthodontic movement of the mandibular second molar into the extraction site of the mandibular first molar. The fixed orthodontic devices included active superelastic coil springs (200 cN) and TADs in the mandibular alveolar bone. Blinding was performed for the subjects and the outcome assessor. The treatment group received 1 shock-wave application with 1000 impulses at 0.19 to 0.23 mJ per square millimeter in the region of the TADs. The placebo group was treated with a deactivated shock-wave applicator and acoustic sham. The TADs positions were evaluated at placement and after 4 months. The reliability and precision of the impression process of the TADs were evaluated in an in-vitro model. Results: Thirteen participants finished the investigation successfully in the treatment group but only 12 finished in the placebo group because 1 TAD loosened. The difference of the total TAD displacement for the 4-month time period between the placebo and treatment groups was 0.17 +/- 0.95 mm (95% CI: -0.96, 0.62). No statistically significant difference between the 2 groups was found when sex was evaluated. Primary stability of the TADs as measured by placement torque, amount of tooth movement, and age of the patients did not influence displacement of the TADs. The reliability and precision of TAD impressions were confirmed. No unintended pernicious effects occurred after shock-wave treatment during the study period. Conclusions: A single application of extracorporeal shock-wave treatment did not improve the stability of the TADs during orthodontic loading. Sufficient interradicular space should be provided to minimize the risk of periodontal and dental root defects. Registration: This trial was registered at https://clinicaltrials.gov. Protocol:Theprotocol was published before trial commencement, NCT01695928. Funding: No funding or conflict of interest to be declared.
机译:简介:在这项随机,安慰剂对照的临床试验中,我们研究了无创体外冲击波对正畸负荷下临时锚固装置(TAD)稳定性的影响。方法:这项在奥地利维也纳的Bernhard Gottlieb大学诊所的30名成年正畸患者参加了这项临床试验,并按1:1的比例按区组随机分配(大小为4)分配给治疗组或安慰剂组。使用软件进行随机化,并将分配隐藏在密封的信封中。入选标准包括健康成人患者,其将下颌第二磨牙进行正畸正畸运动至下颌第一磨牙的取出部位。固定的正畸装置包括活动的超弹性螺旋弹簧(200 cN)和下颌牙槽骨中的TAD。对受试者和结果评估者进行致盲。治疗组在TAD区域接受了1次冲击波施加,每平方毫米0.19至0.23 mJ施加了1000次脉冲。安慰剂组用停用的冲击波施加器和假声治疗。在安置时和4个月后评估TAD的位置。在体外模型中评估了TAD印模过程的可靠性和准确性。结果:治疗组中有13名参与者成功完成了调查,而安慰剂组中只有12名参与者完成了调查,因为1个TAD松动了。安慰剂组和治疗组之间4个月时间的总TAD位移差异为0.17 +/- 0.95毫米(95%CI:-0.96,0.62)。评估性别后,两组之间没有统计学上的显着差异。通过放置扭矩,牙齿移动量和患者年龄测量的TAD的基本稳定性不会影响TAD的位移。 TAD印模的可靠性和准确性得到确认。在研究期间,冲击波治疗后未发生意外的有害影响。结论:单次应用体外冲击波治疗并不能改善正畸加载过程中TAD的稳定性。应提供足够的根际间隙,以最大程度地减少牙周和牙根缺损的风险。注册:该试验已在https://clinicaltrials.gov注册。方案:该协议在试验开始前已发布,NCT01695928。资金:无需宣布资金或利益冲突。

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