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临床试验/ISRCTN50850043
ISRCTN50850043已完成未知

Pragmatic multi-centre randomised trial of surgical versus non-surgical treatment for proximal fracture of the humerus in adults

Teesside University0 个研究点目标入组 250 人开始时间: 2008年3月25日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
250

研究概览

简要总结

2009 Protocol article in http://www.ncbi.nlm.nih.gov/pubmed/19917097 protocol 2014 Results article in https://www.ncbi.nlm.nih.gov/pubmed/25519445 results 2015 Results article in http://www.ncbi.nlm.nih.gov/pubmed/25822598 results 2015 Results article in http://www.ncbi.nlm.nih.gov/pubmed/25756440 results 2016 Results article in http://www.ncbi.nlm.nih.gov/pubmed/26850418 results 2016 Results article in https://www.ncbi.nlm.nih.gov/pubmed/26549433 results 2016 Results article in https://www.ncbi.nlm.nih.gov/pubmed/27756739 results 2020 Other publications in https://www.ncbi.nlm.nih.gov/pubmed/32041811 commentary (added 12/02/2020) 2021 Other publications in https://pubmed.ncbi.nlm.nih.gov/34407641/ cost-effectiveness analysis (added 15/12/2021)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged 16 or above, male and female
  • 2. Presenting to the participating trauma centre within 3 weeks of their injury
  • 3. Radiologically confirmed displaced fracture of the proximal humerus involving the surgical neck
  • 4. Surgeon would consider surgical treatment for the fracture

排除标准

  • 1. Open fracture
  • 2. Cognitive impairment that would preclude participation
  • 3. Co-morbidities precluding surgery/ anaesthesia
  • 4. Clear indication for surgery such as severe soft-tissue compromise requiring surgery/ emergency treatment
  • 5. Multiple injuries: Same limb fractures, other upper limb fractures
  • 6. Pathological fractures (other than osteoporotic)
  • 7. Terminal illness
  • 8. Participant not resident in trauma-centre catchment area

研究者

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