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临床试验/NCT04793971
NCT04793971已完成不适用

Minimal Invasive Treatment of Achilles Tendinopathy: Focus on Percutaneous Release (Maffulli)

Universitaire Ziekenhuizen KU Leuven1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2014年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
8
试验地点
1
主要终点
VISA-A-score

研究概览

简要总结

To evaluate the outcome of percutaneous paratenon release for chronic midportion Achilles tendinopathy.

详细描述

Since 2011 the percutaneous procedure took the place of the open release of the paratenon for the surgical treatment for chronic midportion Achilles tendinopathy in the investigators' center. In this study the investigators re-evaluate the patients undergoing percutaneous surgery since then in order to compare the outcome with the excellent results cited in literature. The patients will be contacted and asked to participate completing a VAS-score, a VISA-A score and agreeing with a clinical examination.

Approving by the Ethical Committee of UZLeuven is pending.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者

入选标准

  • patients that underwent percutaneous paratenon release for chronic midportion Achilles tendinopathy

排除标准

  • insertional tendinopathy
  • open intervention
  • (partial) Achilles tendon rupture

结局指标

主要结局

VISA-A-score

时间窗: 3 months

specific questionnaire about (mal-)function of Achilles tendon

次要结局

  • SF-36-score(3 months)
  • VAS-score(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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