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临床试验/NCT04263493
NCT04263493已完成不适用

Delayed Loading Following Repair of a Ruptured Achilles Tendon - a Randomized Controlled Trial

Bispebjerg Hospital2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2020年5月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
48
试验地点
2
主要终点
Heel-rise test

研究概览

简要总结

The purpose of the study is to investigate if delayed loading following surgical treated Achilles tendon rupture influence the clinical outcome and muscle and tendon structure after one year.

The investigators hypothesize that delaying the gradual introduction of loading in the initial 26 weeks may reduce the heel-rise deficit (primary outcome) and thus improve the clinical outcome one year after surgery (primary endpoint).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with a traumatic, complete mid-substance Achilles tendon
  • No contraindications for MRI
  • Presented within 14 days from injury
  • Adult (18 to 60 years)
  • Understand Danish
  • Manage transport to/from the hospital on their own

排除标准

  • Other injuries affecting their lower limb functions
  • Prior Achilles tendon Rupture
  • Systemic diseases influencing tendon healing
  • Anticoagulation treatment
  • Inability to follow rehabilitation or complete follow-ups
  • Immunosuppressive treatment including systematic corticosteroid treatment

结局指标

主要结局

Heel-rise test

时间窗: One-year follow-up

Heel-rise height deficit on the injured side relative to the uninjured side

次要结局

  • Tendon length and cross-sectional area(1 week, 3 months, 6 months and 1 year)
  • The Achilles tendon rupture score (ATRS)(Recall before injury and 1 year)
  • Muscle fascicle length and doppler activity in the tendon(2 weeks, 3 months, 6 months and 1 year)
  • Isokinetic plantar flexion muscle strength(1 year)
  • Physical activity level(Recall before injury and 1 year)
  • Heel-rise work(6 months and 1 year)
  • The Achilles tendon resting angle (ATRA)(2 weeks, 3 months, 6 months and 1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rikke Høffner

PhD student, MSc, PT

Bispebjerg Hospital

研究点 (2)

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