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临床试验/DRKS00024923
DRKS00024923尚未招募未知

Validation of the three-dimensional scoliosis therapy according to Katharina Schroth for adolescent idiopathic scoliosis using a newly introduced radiation-free sonographic measurement method - Scolioscan®.

Asklepios Katharina-Schroth Klinik0 个研究点目标入组 240 人开始时间: 2021年5月5日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
240

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
10 Years 至 18 Years(—)
性别
All

入选标准

  • adolescent idiopathic scoliosis
  • 10-18 years
  • four-week rehabilitation or presentation at the outpatient clinic of the Asklepios Katharina-Schroth-clinic

排除标准

  • neuromuscular scolioses
  • congenital scolioses
  • infantile and juvenile scoliosis
  • secondary scolioses
  • patients with mental retardation
  • patients with spinal fusion surgery
  • patients with reported pain at rest above a score of 5 on the visual analogue scale from 0 (no pain) to 10 (most severe pain imaginable)
  • patients with an acute medical condition, such as fever, unhealed injuries, dizziness, nausea or balance problems
  • patients taking medications that affect vigilance, muscle tone or the central nervous system
  • patients who are (possibly) pregnant
  • patients who do not have the capacity to give consent or to be informed, unless this condition is due to their age and there is informed consent from their legal representative or guardian.
  • patients with a BMI >23 kg/m² (27)
  • patients with a scoliosis > 50°(1, 27)
  • high thoracic scolioses with a vertebra between TH2 and TH6

研究者

发起方
Asklepios Katharina-Schroth Klinik

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