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Evaluating hearing performance with cochlear implants within the same patient using daily randomization and imaging-based fitting - The ELEPHANT study

机译:使用每日随机化和基于成像的拟合 - 大象研究评估同一患者内的耳蜗植入物的听力表现 - 大象研究

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BACKGROUND:Prospective research in the field of cochlear implants is hampered by methodological issues and small sample sizes. The ELEPHANT study presents an alternative clinical trial design with a daily randomized approach evaluating individualized tonotopical fitting of a cochlear implant (CI).METHODS:A single-blinded, daily-randomized clinical trial will be implemented to evaluate a new imaging-based CI mapping strategy. A minimum of 20 participants will be included from the start of the rehabilitation process with a 1-year follow-up period. Based on a post-operative cone beam CT scan (CBCT), mapping of electrical input will be aligned to natural place-pitch arrangement in the individual cochlea. The CI's frequency allocation table will be adjusted to match the electrical stimulation of frequencies as closely as possible to corresponding acoustic locations in the cochlea. A randomization scheme will be implemented whereby the participant, blinded to the intervention allocation, crosses over between the experimental and standard fitting program on a daily basis, and thus effectively acts as his own control, followed by a period of free choice between both maps to incorporate patient preference. With this new approach the occurrence of a first-order carryover effect and a limited sample size is addressed.DISCUSSION:The experimental fitting strategy is thought to give rise to a steeper learning curve, result in better performance in challenging listening situations, improve sound quality, better complement residual acoustic hearing in the contralateral ear and be preferred by recipients of a CI. Concurrently, the suitability of the novel trial design will be considered in investigating these hypotheses.TRIAL REGISTRATION:ClinicalTrials.gov: NCT03892941. Registered 27 March 2019.
机译:背景:耳蜗植入物领域的前瞻性研究受到方法问题和小样本尺寸的阻碍。大象研究提出了一种替代的临床试验设计,具有日常随机方法,评估耳蜗植入物的个性化型仪表拟合(CI)。方法:将实施单一盲,日常随机临床试验,以评估一种新的成像基于CI映射战略。至少有20名参与者将在康复过程的开始时包括1年的随访期。基于操作后锥形光束CT扫描(CBCT),电输入的映射将与各个耳蜗中的自然距离排列对齐。将调整CI的频率分配表以尽可能地将频率的电刺激与耳蜗中的相应声学位置相匹配。将实施随机化方案,其中参与者对干预分配蒙蔽,每天在实验和标准拟合程序之间交叉,从而有效地作为他自己的控制,其次是两张地图之间的自由选择纳入患者偏好。通过这种新方法,已经解决了一阶核算效果和有限的样本大小的发生。探讨:实验拟合策略被认为导致更陡峭的学习曲线,导致更好的性能在挑战的听力情况下,提高音质,更好地补充在对侧耳中的残留声学听力,并通过CI的受体优选。同时,在调查这些假设时,将考虑新的试验设计的适用性.TRIAL注册:ClinicalTrials.gov:NCT03892941。注册2019年3月27日。

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