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首页> 外文期刊>BMC Musculoskeletal Disorders >Nordic Innovative Trial to Evaluate OsteoPorotic Fractures (NITEP-group): non-operative treatment versus surgery with volar locking plate in the treatment of distal radius fracture in patients aged 65 and over – a study protocol for a prospective, randomized controlled trial
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Nordic Innovative Trial to Evaluate OsteoPorotic Fractures (NITEP-group): non-operative treatment versus surgery with volar locking plate in the treatment of distal radius fracture in patients aged 65 and over – a study protocol for a prospective, randomized controlled trial

机译:北欧评估骨质疏松性骨折的创新试验(NITEP组):非手术治疗与手掌锁定钢板手术治疗65岁及以上患者的radius骨远端骨折–一项前瞻性,随机对照试验的研究方案

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摘要

In the literature, there are numerous studies that compare different surgical procedures in the treatment of distal radius fractures (DRF). It is, however, unknown whether operative treatment and better restoration of anatomy with volar locking plate yields a better functional outcome in the elderly population when compared with non-operative treatment. This study is a prospective, randomized, controlled, multi-center trial. The purpose will be to compare the non-operative and operative treatment of initially or early malaligned distal radius fractures in patients aged 65 and older. The primary outcome in this study will be the patient rated wrist evaluation (PRWE) score measured after 1 and 2 years. We expect that initial operative treatment of a DRF with volar locking plate will not yield superior results when compared with non-operative treatment with cast immobilization in terms of functional outcome, pain, disability, quality of life, grip strength, and number of complications. This trial is registered on clinicaltrials.gov , identifier NCT02879656 , registration date 08/17/2016.
机译:在文献中,有许多研究比较了radius骨远端骨折(DRF)的不同手术方法。然而,与非手术治疗相比,在老年人口中,手术治疗和采用掌侧锁定钢板更好地恢复解剖结构是否会产生更好的功能结局还不得而知。这项研究是一项前瞻性,随机,对照,多中心试验。目的是比较65岁及65岁以上患者radius骨远端或远端早期骨折的非手术和手术治疗方法。这项研究的主要结果将是患者在1年和2年后测得的腕关节评估(PRWE)评分。我们希望,与功能固定结节的非手术治疗相比,使用掌侧锁定板进行DRF的初始手术治疗不会产生更好的结果,无论是在功能预后,疼痛,残疾,生活质量,抓地力和并发症数量方面。该试验已在Clinicaltrials.gov上注册,标识为NCT02879656,注册日期为2016年8月17日。

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