Clinical Validation and Testing of Percutaneous Cochlear Implantation
Clinical Validation and Testing of Percutaneous Cochlear Implantation
批准号:
8668921
负责人:
ROBERT F LABADIE
金额:
$60.85万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-04-05 至 2017-06-30
关键词:
AbdomenAcoustic NerveAdultAmericanAnatomyCaliberClinicalClinical ProtocolsClinical TrialsCochleaCochlear ImplantsCochlear implant procedureComputer softwareCost MeasuresCustomDevelopmentDevicesDiagnosisDissectionElectrodesEndoscopesEquipmentExcisionExhibitsExternal EarFacial nerve structureFundingGoalsGuidelinesHeadHealedHearingHearing Impaired PersonsHourImageImplanted ElectrodesIndividualInjuryInstitutional Review BoardsInterventionLabyrinthLaparoscopic Surgical ProceduresLateralLocal anesthesiaLocationMastoid processMeasurableMeasuresMedical DeviceMetricOperating RoomsOperative Surgical ProceduresPatientsPeer ReviewPhasePhase II Clinical TrialsPostoperative PeriodProceduresProgress ReportsProtocols documentationPublicationsRandomized Clinical TrialsRecoveryRecovery RoomResearchResectedRiskSafetyScala TympaniServicesSurfaceSurrogate EndpointTechniquesTechnologyTestingTimeTissuesUnited StatesUnited States National Institutes of HealthValidationVisitVisualWorkbonecostcraniumdesignhealinghearing impairmentinstrumentminimally invasivenovel strategiesphase 1 studyphase 2 studyrandomized trialresearch clinical testingstandard of caretooltrial comparingusability
中文摘要
描述(由申请人提供):人工耳蜗术需要接触到内耳,特别是耳蜗,在这种手术中,使用电极阵列来刺激听神经,使聋人能够听到。已在全球放置了超过240,000个CI,其中约70,000个在美国执行。预测表明,多达75万患有严重听力损失的美国人可能会从CI中受益。在我们正在进行的NIH资助的项目(R01DC008408)中,我们已经证明了经皮人工耳蜗术(PCI)的可行性。经皮冠状动脉介入术将CI手术简化为从侧颅表面到耳蜗单一次钻孔。钻探路径的规划和执行使用了图像引导技术,以避免重要的邻近解剖(例如面神经),并击中目标-耳蜗鼓阶。在临床试验中,我们已经在31名成人患者身上验证了经皮冠状动脉介入治疗技术,统计预测表明,避免重要解剖的比率与传统手术相似。此外,我们已经通过开发钻探仪器和技术开始实施经皮冠状动脉介入治疗,并对另外10名患者进行了逐渐加深的钻探,其中最新的患者进行了完全经皮冠状动脉介入治疗。经皮冠状动脉介入治疗的潜在好处很多,包括更少的组织切除和更短的手术时间。在附上的意见书中,我们建议在我们成功开发经皮冠状动脉介入治疗的基础上,通过(I)将我们的第一阶段研究延长一年以产生可靠的临床方案,以及(Ii)进行由随机临床试验比较组成的第二阶段研究,以探索潜在的好处
经皮冠状动脉介入治疗对传统脑梗塞手术的影响。更具体地说,在第一阶段,我们将(A)进一步改进我们的成像和规划软件,以优化准确性和可用性,(B)实施冗余的安全检查,以最大限度地减少对面神经的损伤风险,(C)研究通过经皮冠状动脉腔内成形术进入耳蜗口的三种选择,并为最终方案选择最佳方案,(D)调查使用内窥镜来验证Scala的准确靶向
(E)完成用于最终CI电极放置的插入工具的设计。在第二阶段随机试验中,我们将面对面地比较传统的CI和PCI手术,正式的终点是(A)介入期间切除的组织数量和(B)介入的时间。这些正式指标将被用来评估(A)手术对个别患者的影响,这可能预示着PCI患者更快的恢复和更快的CI激活,以及(B)尽管需要
由于手术时间的减少,额外的设备对于经皮冠状动脉介入治疗来说可能更便宜。虽然我们的研究旨在证明组织切除的体积和介入时间在统计上都有显著减少,但我们仍将对其他潜在的好处持开放态度(例如,通过经皮冠状动脉介入治疗在鼓阶放置更一致的电极)。如果我们的研究成功,我们认为经皮冠状动脉介入治疗将成为脑梗塞的首选技术。
英文摘要
DESCRIPTION (provided by applicant): Access to the inner ear, specifically the cochlea, is required for cochlear implant (CI) surgery, in which an electrode array is used to stimulate the auditory nerve and allow deaf people to hear. More than 240,000 CIs have been placed worldwide with approximately 70,000 performed in the USA. Projections indicate that up to 750,000 Americans with severe hearing loss may benefit from CI. In our ongoing NIH-funded project (R01 DC008408), we have demonstrated the feasibility of percutaneous cochlear implantation (PCI). PCI reduces CI surgery to a single pass of a drill from the lateral skull surface to the cochlea. The drill path is planned and executed using image-guided technology so as to avoid vital adjacent anatomy (e.g. the facial nerve) and hit the target-the scala tympani of the cochlea. In clinical trials we have validated the PCI technique on 31 adult patients with statistical projections indicating avoidance of vital anatomy at a rate similar to that of traditioal surgery. Furthermore, we have begun implementation of PCI by developing instruments and techniques for drilling and have performed incrementally deeper drilling on 10 additional patients the most recent of which had complete PCI performed. The potential benefits of PCI are many including less tissue removal and shorter time of surgical intervention. In the attached submission, we propose to build on our successful development of PCI and explore potential benefits by (i) extending our Phase I study by one year in order to produce a robust clinical protocol and (ii) carrying out a Phase II study consisting of a randomized clinical trial comparing
PCI to traditional CI surgery. More specifically, during Phase I we will (a) further refine our imaging and planning software to optimize accuracy and usability, (b) implement redundant safety checks to minimize risk of injury to the facial nerve, (c) investigate three options for creating the opening into the cochlea via the PCI track and picking the best one for the final protocol, (d) investigate the use of endoscopes for verification of accurate targeting of the scala
tympani component of the cochlea, and (e) finalize design of an insertion tool for final CI electrode placement. In the Phase II randomized trial we will compare, head-to-head, traditional CI and PCI surgery with formal endpoints being (a) amount of tissue resected during intervention and (b) time of intervention. These formal metrics will be used to assess (a) the impact of the procedure on individual patients, which may portend quicker recovery and quicker CI activation for PCI patients, and (b) the overall cost of intervention which despite the need for
additional equipment may be cheaper for PCI due to decreased operative time. While our study is set up to demonstrate statistically significant reductions in both volume of tissue removed and time of intervention, we will remain open to other potential benefits (e.g. more consistent electrode placement in the scala tympani with PCI). If our study is successful, we posit that PCI will become the preferred technique for CI.
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