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临床试验/NL-OMON45575
NL-OMON45575已完成不适用

Clinical usability of non-contact scanners in measuring stumpvolume of transtibial amputee patients - CCUNCMSTAP

Isala Klinieken0 个研究点目标入组 36 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
36

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • •Uni- or bilateral transtibial amputation
  • •Operation of the stump more than 1 year ago
  • •Older than 18 years
  • •Informed consent
  • •Availability at research data

排除标准

  • •Less than 1 year ago an operation of the stump
  • •Large changes in stump volume during the day with co-morbidity like heart failure, kidney failure, deep vein thrombosis, lymphedema, fracture of the leg, rheumatoid artritis, CRPS, dermatologic diseases associated with edema.
  • •Wound at the stump of more than 1 cm amplitude and/or signs of infection, in which clinically may be assumed that this will influence the stumpvolume
  • •Weakness of upperleg which causes inability to lift the leg up in the air
  • •Not able to make a transfer from (wheel)chair to research table
  • •Not enough understanding of the Dutch language to give answer to simple questions, follow simple instructions or understand the informed consent letter

研究者

发起方
Isala Klinieken

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