ISRCTN10649958已完成未知
A randomised controlled trial of surgical versus non-surgical treatment of lateral compression injuries of the pelvis with complete sacral fractures (LC1) in the non-fragility fracture patient - a feasibility study
orth Bristol NHS Trust0 个研究点目标入组 37 人开始时间: 2018年8月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 37
研究概览
简要总结
2020 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/32047021 protocol (added 13/02/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. LC1 fracture with complete sacral fracture
- •2. 16 years and older
排除标准
- •Current participant exclusion criteria as of 06/08/2019:
- •1. Unable to be randomised within 72 hours of having capacity to comprehend the study information following arrival at the major trauma centre
- •2. Fragility fractures resulting from low-energy trauma (fall from less than standing height)
- •3. Presenting medical condition which precludes surgical intervention
- •4. Unable to provide informed consent
- •Previous participant exclusion criteria:
- •1. No bony anterior pelvic ring injury
- •2. Unable to be randomised within 2 weeks of injury
- •3. Unable to mobilise for 6 metres prior to injury
- •4. Fragility fractures resulting from low-energy trauma (fall from less than standing height)
- •5. Unfit for anaesthesia
- •6. Unable to provide informed consent
- •7. Unable to adhere to Protocol
研究者
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