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临床试验/NCT03611244
NCT03611244招募中不适用

Prevention of Scoliosis in Patients With Duchenne Muscular Dystrophy Using Portable Seat Device Devised to Maintain Lumbar Lordosis : 5 Year Follow up Study

Seoul National University Hospital3 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2018年8月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
98
试验地点
3
主要终点
Incidence of scoliosis

研究概览

简要总结

This study will be conducted without blind method. The portable seat device devised to maintain lumbar lordosis will be made within 1 year after the loss of ambulation in the participants with Duchenne muscular dystrophy with prospective design.

In the control group, the presence of scoliosis will be calculated 5 years after the loss of ambulation in participants with Duchenne muscular dystrophy through analysis of retrospective medical records who had not been applied the portable seat device.

详细描述

In the retrospective data of Seoul National University Children's Hospital, the incidence of 5-year scoliosis in the control group in the past using steroids alone was 70% in patients with confirmed Duchenne muscular dystrophy. When applying the portable seat device (experimental group), the incidence of scoliosis is expected to decrease to 50% (ie, 35% because of 50% of 70%) compared with using steroid alone.

In this study, investigators will enroll 70 control subjects who did not use the portable seat device through retrospective data. The number of subjects required to show the difference between the significance level of 5% and the power of 80% was 19, and 28 participants with DMD are required considering 30% dropout rate.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
7 Years 至 15 Years(Child)
性别
Male
接受健康志愿者

入选标准

  • Patients with the diagnosis of Duchenne muscular dystrophy diagnosed by genetic study were included.
  • Within 1 year after loss of ambulation (Vignos scale 7 points or more)
  • Condition without scoliosis
  • Conditions that do not have physical (eg, cerebral palsy) and mental (eg, moderate or higher intellectual disability) comorbid conditions that will affect the use of postural seat device.

排除标准

  • Patients who do not agree to participate in this study
  • Patients not taking steroids
  • Patient with scoliosis

研究组 & 干预措施

Experimental group

Experimental

When loss of ambulation was observed in patients with Duchenne muscular dystrophy, portable seat device devised to maintain lumbar lordosis were applied within 1 year, and then compliance with the the device were evaluated at 6-month intervals for 5 years.

干预措施: Portable seat device devised to maintain lumbar lordosis (Device)

Control group

No Intervention

Analysis of retrospective medical records who had not been applied portable seat device devised to maintain lumbar lordosis

结局指标

主要结局

Incidence of scoliosis

时间窗: 5 years after loss of ambulation

Frequency of scoliosis more than 10 degrees on spine x-ray on supine position

次要结局

  • Incidence of scoliosis("Day 0", "Month 6" "Month 12" "Month 18" "Month 24" "Month 30" "Month 36" "Month 42" "Month 48" "Month 54" "Month 60")

研究者

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

Hyung-ik Shin

Associate professor

Seoul National University Hospital

研究点 (3)

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