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首页> 外文期刊>Trials >Comparison of 22G standard and Franseen needles in endoscopic ultrasound-guided fine-needle aspiration for diagnosing pancreatic mass lesions: Study protocol for a controlled trial
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Comparison of 22G standard and Franseen needles in endoscopic ultrasound-guided fine-needle aspiration for diagnosing pancreatic mass lesions: Study protocol for a controlled trial

机译:22G标准和Franseen针在内窥镜超声引导的细针觉得诊断胰腺大众病变中的比较:对照试验的研究方案

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BACKGROUND:Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) was developed with the aim of further improving the diagnostic performance of endoscopic ultrasound. Although novel puncture needles have been specifically designed for collecting sufficient tissue specimens, clinical studies have indicated no clear difference in diagnostic performance between these novel needles and conventional puncture needles. Recently, a needle with Franseen geometry was developed specifically for EUS-FNA biopsy. Due to the characteristic shape of its tip, the Franseen needle is expected to be effective for scraping tissues, thus potentially increasing the diagnostic accuracy of EUS-FNA biopsy. We plan to carry out a prospective, multicenter, open-labeled, controlled trial to compare conventional and Franseen needles in terms of the diagnostic accuracy of EUS-FNA for evaluating the malignancy of pancreatic mass lesions.METHODS/DESIGN:The study will enroll 520 patients with pancreatic mass managed at any of 21 participating endoscopic centers. Lesion samples obtained using 22G conventional and Franseen needles will be assessed to compare the efficacy and safety of these two types of needles in EUS-FNA for evaluating the malignancy of mass lesions in the pancreas. Tissue samples will be fixed in formalin and processed for histologic evaluation. For the purpose of this study, only samples obtained with the first needle pass will be used for comparing the: (i) accuracy of the malignancy diagnosis, (ii) sensitivity and specificity for the malignancy diagnosis, (iii) procedure completion rate, (iv) sample cellularity, and (v) incidence of complications. Patient enrollment begins on July 17, 2018.DISCUSSION:The outcomes of this study may provide insight into the optimal needle choice for evaluating the malignancy of pancreatic solid lesions, thus aiding in the development of practice guidelines for pancreatic diseases.TRIAL REGISTRATION:University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR), UMIN000030634. Registered on 29 December 2017. http://www.umin.ac.jp/ Version number: 01.2017.12.28.
机译:背景:具有进一步提高内窥镜超声的诊断性能的目的,开发了内窥镜超声引导的细针吹口(EUS-FNA)。虽然新颖的穿刺针专门用于收集足够的组织标本,但临床研究表明这些新颖针和常规穿刺针之间的诊断性能没有明显差异。最近,具有Franseen几何形状的针专为EUS-FNA活检开发。由于其尖端的特征形状,预期弗兰森针对刮削组织有效,因此可能增加了EUS-FNA活检的诊断准确性。我们计划在EUS-FNA诊断准确性评估胰腺质量病变的恶性肿瘤的诊断准确性方面进行预期,多中心,开放式,受控试验,以比较常规和弗兰森针比较胰腺炎病变恶性肿瘤。方法/设计:该研究将注册520胰腺质量的患者在21个参与内窥镜中心中的任何一个中管理。将评估使用22g常规和弗兰森针获得的病变样品,以比较这两种类型针对EUS-FNA的疗效和安全性,以评估胰腺中质量病变的恶性肿瘤。组织样品将固定在福尔马林中并加工用于组织学评估。出于本研究的目的,仅使用第一针通差获得的样品将用于比较:(i)恶性诊断的准确性,(ii)恶性诊断的敏感性和特异性,(iii)程序完成率( iv)样品细胞,和(v)并发症的发生率。患者入学员于2018年7月17日开始。探讨:本研究的结果可以深入了解评估胰腺固体病变恶性的最佳针头选择,从而有助于开发胰腺疾病的实践指南.TRIAL注册:大学医院医疗信息网络临床试验登记处(UMIN-CTR),UMIN000030634。 2017年12月29日注册。http://www.umin.ac.jp/版本号:01.2017.12.28。

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