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首页> 外文期刊>Trials >Hernia reduction following laparotomy using small stitch abdominal wall closure with and without mesh augmentation (the HULC trial): study protocol for a randomized controlled trial
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Hernia reduction following laparotomy using small stitch abdominal wall closure with and without mesh augmentation (the HULC trial): study protocol for a randomized controlled trial

机译:使用小针脚壁闭合术后腹膜切开术,其中没有网眼壁闭合(Hulc试验):随机对照试验的研究方案

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BACKGROUND:Incisional hernias are among the most frequent complications following abdominal surgery and cause substantial morbidity, impaired health-related quality of life and costs. Despite improvements in abdominal wall closure techniques, the risk for developing an incisional hernia is reported to be between 10 and 30% following midline laparotomies. There have been two recent innovations with promising results to reduce hernia risks, namely the small stitches technique and the placement of a prophylactic mesh. So far, these two techniques have not been evaluated in combination.METHODS:The HULC trial is a multicentre, randomized controlled, observer- and patient-blinded surgical effectiveness trial with two parallel study groups. A total of 812 patients scheduled for elective abdominal surgery via a midline laparotomy will be randomized in 12 centres after informed consent. Patients will be randomly assigned to the control group receiving closure of the midline incision with a slowly absorbable monofilament suture in the small stitches technique or to the intervention group, who will receive a small stitches closure followed by augmentation with a light-weight polypropylene mesh in the onlay technique. The primary endpoint will be the occurrence of incisional hernias, as defined by the European Hernia Society, within 24?months after surgery. Further perioperative parameters, as well as patient-reported outcomes, will be analysed as secondary outcomes.DISCUSSION:The HULC trial will address the yet unanswered question of whether a combination of small stitched fascial closure and onlay mesh augmentation after elective midline laparotomies reduces the risk of incisional hernias. The HULC trial marks the logical and innovative next step in the development of a safe abdominal closure technique.TRIAL REGISTRATION:German Clinical Trials Register, DRKS00017517. Registered on 24th June 2019.
机译:背景:切口疝是腹部手术后最常见的并发症,并导致大量发病率,有关的健康状生活质量和成本。尽管腹壁闭合技术有所改善,但据报道,在中线腹腔切开术后,据报道,发展切口疝的风险在10%至30%之间。最近有两种创新,有希望的结果减少疝气风险,即小针脚技术和预防性网格的放置。到目前为止,这两种技术尚未组合评估。方法:Hulc试验是一种用两个平行研究组的多期,随机控制,观察者和患者盲目的手术效果试验。通过中线剖腹手术预定612名患者,在知情同意后12个中心将在12个中心随机化。患者将随机分配给接受中线切口的对照组,在小针脚技术或干预组中使用缓慢的可吸收的单丝缝合物,他们将收到一个小针脚,然后用轻量级聚丙烯网进行增强镶嵌技术。主要终点将是欧洲疝气社会定义的切口疝的发生,在手术后24个月内。将分析进一步的围手术期参数,以及患者报告的结果将被分析为次要的结果。讨论:赫尔卡氏试验将解决选修中线剖腹产后小缝缝合闭合和围栏网格增强的尚未答复的问题是否降低了风险切口疝气。 HULC试验标志着安全腹部闭合技术开发的逻辑和创新.TRIAL注册:德国临床试验登记,DRKS00017517。 2019年6月24日注册。

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