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首页> 外文期刊>BJU international >The impact of targeted training, a dedicated protocol and on-site training material in reducing observer variability of prostate and transition zone dimensions measured by transrectal ultrasonography, in multicentre multinational clinical trials of m
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The impact of targeted training, a dedicated protocol and on-site training material in reducing observer variability of prostate and transition zone dimensions measured by transrectal ultrasonography, in multicentre multinational clinical trials of m

机译:在m的多中心跨国临床试验中,针对性培训,专用协议和现场培训材料在减少观察者变异性和经直肠超声检查所测量的前列腺和过渡区尺寸方面的影响

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OBJECTIVE: To assess the variability of a standardized protocol of transrectal ultrasonography (TRUS), with targeted training, and compare it to the variability in other multicentre clinical trials, as TRUS-estimated total prostate volume (TPV) and transition zone volume (TZV) are considered important efficacy endpoints in assessing new drug therapies for benign prostatic enlargement (BPE), but standardizing TRUS remains a challenge in such studies. PATIENTS AND METHODS: In all, 174 patients with BPE in the placebo arm of a 30-centre clinical trial were analysed at baseline, 13 and 26 weeks with TRUS, to extract TPV and TZV values. All TRUS operators received training in the standardized methods, which was supplemented at the outset by a compact disc-based video. RESULTS: The mean (sd) changes from baseline in TPV at 13 and 26 weeks were - 2.9 (8.9) and -1.9 (8.5) mL, respectively; the respective mean changes from baseline in TZV were -1.2 (6.4) and + 0.7 (7.8) mL. For TPV, 80% of the measurements had differences of + 5.2 to -13.4 mL at 13 weeks, and + 8.0 to - 10.9 mL at 26 weeks. For TZV, 80% of the differences were + 5.8 to - 7.4 at 13 weeks, and + 9.3 to -6.5 mL at 26 weeks. CONCLUSION: The performance of TRUS compared favourably with similar published multicentre studies, which we suggest relates in part to the careful implementation of the protocol. We showed that diligent implementation of a detailed protocol, supplemented by targeted training of investigators and provision of on-site training material, promoted consistent acquisition and successful derivation of key clinical trial endpoints. Quantifying the variability of such endpoints will enable us to track deployment quality for future clinical trials, and will ensure that trials are sufficiently powered to define small changes in prostate size.
机译:目的:评估经靶标训练的经直肠超声检查(TRUS)的标准化方案的变异性,并将其与其他多中心临床试验中的变异性进行比较,如TRUS估算的总前列腺体积(TPV)和过渡区体积(TZV)被认为是评估良性前列腺增生(BPE)的新药疗法的重要疗效终点,但是在此类研究中标准化TRUS仍然是一个挑战。患者和方法:总共在一项30中心临床试验的安慰剂组中对174例BPE患者在基线,TRUS的13周和26周进行了分析,以提取TPV和TZV值。所有TRUS操作员都接受了标准化方法的培训,并且在一开始就获得了基于光盘的视频的补充。结果:TPV在第13和26周时相对于基线的平均(sd)变化分别为-2.9(8.9)和-1.9(8.5)mL; TZV相对于基线的平均变化分别为-1.2(6.4)和+ 0.7(7.8)mL。对于TPV,在13周时,80%的测量值差异为+ 5.2至-13.4 mL,在26周时为+ 8.0至-10.9 mL。对于TZV,在13周时,差异的80%为+ 5.8至-7.4,而在26周时,差异为+ 9.3至-6.5 mL。结论:TRUS的性能优于类似的已发表的多中心研究,我们建议在某种程度上与协议的认真实施有关。我们表明,认真实施详细的协议,再加上针对研究人员的有针对性的培训以及提供现场培训材料,可以促进关键临床试验终点的持续获取和成功推导。量化这些端点的变异性将使我们能够跟踪未来临床试验的部署质量,并确保试验具有足够的能力来定义前列腺大小的微小变化。

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