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首页> 外文期刊>BMC Musculoskeletal Disorders >Routine versus on demand removal of the syndesmotic screw; a protocol for an international randomised controlled trial (RODEO-trial)
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Routine versus on demand removal of the syndesmotic screw; a protocol for an international randomised controlled trial (RODEO-trial)

机译:常规与按需去除股骨螺钉国际随机对照试验(RODEO-trial)的协议

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Syndesmotic injuries are common and their incidence is rising. In case of surgical fixation of the syndesmosis a metal syndesmotic screw is used most often. It is however unclear whether this screw needs to be removed routinely after the syndesmosis has healed. Traditionally the screw is removed after six to 12 weeks as it is thought to hamper ankle functional and to be a source of pain. Some studies however suggest this is only the case in a minority of patients. We therefore aim to investigate the effect of retaining the syndesmotic screw on functional outcome. This is a pragmatic international multicentre randomised controlled trial in patients with an acute syndesmotic injury for which a metallic syndesmotic screw was placed. Patients will be randomised to either routine removal of the syndesmotic screw or removal on demand. Primary outcome is functional recovery at 12?months measured with the Olerud-Molander Score. Secondary outcomes are quality of life, pain and costs. In total 194 patients will be needed to demonstrate non-inferiority between the two interventions at 80% power and a significance level of 0.025 including 15% loss to follow-up. If removal on demand of the syndesmotic screw is non-inferior to routine removal in terms of functional outcome, this will offer a strong argument to adopt this as standard practice of care. This means that patients will not have to undergo a secondary procedure, leading to less complications and subsequent lower costs. This study was registered at the Netherlands Trial Register (NTR5965), Clinicaltrials.gov ( NCT02896998 ) on July 15th 2016.
机译:上下颌损伤很常见,并且发病率正在上升。在通过手术固定韧带的情况下,最常使用金属韧带螺钉。然而,目前尚不清楚在牙周病愈合后是否需要例行拆除该螺钉。传统上,在六到十二周后将螺钉移除,因为这会妨碍脚踝的功能并引起疼痛。但是,一些研究表明,只有少数患者是这种情况。因此,我们旨在研究保留下颌联合螺钉对功能预后的影响。这是一项实用的国际多中心随机对照试验,用于放置有金属下颌骨螺钉的急性下颌骨损伤的患者。患者将被随机分配到常规去除双下颌联合螺钉或按需去除。主要结果是用Olerud-Molander评分测量的12个月时的功能恢复。次要结果是生活质量,痛苦和成本。总共将需要194名患者在80%的功效和0.025的显着性水平(包括15%的随访损失)下证明两次干预之间的非劣效性。如果就功能结局而言,按需切除下颌联合螺钉的效果不逊于常规切除,则这将为将其作为标准护理方法提供强有力的论据。这意味着患者将不必进行二次手术,从而减少了并发症并降低了成本。这项研究于2016年7月15日在荷兰临床试验注册(NTR5965)的Clinicaltrials.gov(NCT02896998)上进行了注册。

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