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首页> 外文期刊>Clinical oral implants research >6‐mm‐short and 11‐mm‐long implants compared in the full‐arch rehabilitation of the edentulous mandible: A 3‐year multicenter randomized controlled trial
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6‐mm‐short and 11‐mm‐long implants compared in the full‐arch rehabilitation of the edentulous mandible: A 3‐year multicenter randomized controlled trial

机译:6毫米 - 短和11毫米长的植入物在薄拱康复的全拱形康复上比较:3年的多中心随机对照试验

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Abstract Objective The aim of this multicenter parallel‐group randomized controlled trial is to compare 6‐mm‐short with 11‐mm‐long implants in the rehabilitation of totally edentulous mandible in a completely comparable clinical situation, from anatomical, surgical, and prosthetic point of view. Material and methods Thirty patients were selected in three study centers to receive a fixed full‐arch mandibular rehabilitation supported by five inter‐foraminal implants. Patients were randomly allocated, at the time of surgery, half to the test group (6‐mm‐long implants) and half to the control group (11‐mm‐long implants). No bone augmentation procedure was performed. After 3?months, a screw‐retained full‐arch prosthesis with distal cantilevers was positioned (baseline). Peri‐implant marginal bone level change (MBLc), implant and prosthesis survival rate, and biological/technical complications were evaluated after 1 and 3?years. Results Thirty subjects (150 implants) were evaluated after 1?year and 28 (140 implants) after 3?years. No implant or prosthesis loss occurred. No significant inter‐group difference for biological/technical complications was registered. No statistically significant ( p ??.025) intra‐group or inter‐group difference in the mean MBLc values was registered. The mean MBLc was 0.01?±?0.19?mm and ?0.04?±?0.21?mm at 1?year, and ?0.10?±?0.24?mm and 0.02?±?0.25?mm at 3?years (test and control groups, respectively). Conclusions 6‐mm‐short implants may be a reliable option when used in the rehabilitation of total edentulous mandibles. These results need to be confirmed by longer follow‐up data from well‐designed randomized controlled clinical trials.
机译:摘要目的这种多中心并联组随机对照试验的目的是在完全可比较的临床情况下在完全相当的临床情况下恢复6毫米 - 长的植入物,从解剖学,外科和假期点进行康复看法。材料和方法在三个研究中心中选择了30名患者,以获得五个间隔内植入物支持的固定全拱形颌骨康复。在手术时随机分配患者,一半到试验组(长植入物)和对照组(11毫米植入物)。没有进行骨增强程序。 3个月后,定位了具有远端悬臂的螺钉保留的全拱形假体(基线)。 Peri-植入边缘骨水平变化(MBLC),植入和假体存活率,1和3年后评估生物/技术并发症。结果在3年后,在1年和28(140个植入物)后评估了30个受试者(150种植体)。没有发生植入物或假体损失。没有重大群体的生物/技术并发症间差异。没有统计学意义(P?&Δ025)在平均mblc值中,在基础上或组间差异。平均mblc为0.01?±0.19Ω·mm和?0.04?±0.21?±0.21Ω·mm,和?0.10?±0.24?mm和0.02?±0.25?mm在3?年(测试和控制分别群体)。结论在恢复全面的颌骨​​康复时,6毫米短的植入物可能是可靠的选择。这些结果需要通过精心设计的随机对照临床试验来确认较长的后续数据。

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