跳至主要内容
临床试验/NCT03426215
NCT03426215已完成不适用

Observational Study on the Long-Term Course of Integrative Korean Medicine Treatment for Lumbar Intervertebral Disc Herniation: Prospective Multicenter 10 Year Follow-up

Jaseng Medical Foundation1 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2018年3月10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
65
试验地点
1
主要终点
Change in Visual Analogue Scale (VAS) of radiating leg pain

研究概览

简要总结

This observational study will assess the long-term course and effect of Korean medicine treatment in lumbar intervertebral disc herniation patients who received integrative Korean medicine treatment for 24 weeks as part of a previous clinical study.

详细描述

This observational study will assess the long-term course and effect of Korean medicine treatment in lumbar intervertebral disc herniation patients with a main complaint of radiating leg pain who received integrative Korean medicine treatment for 24 weeks at Jaseng Hospital of Korean Medicine (Gangnam main branch) as part of a previous clinical study which was conducted from November, 2006 to April, 2007, and give written informed consent to long-term follow-up assessment at 10 years.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Lumbar intervertebral disc herniation patients with a main complaint of radiating leg pain who received integrative Korean medicine treatment for 24 weeks at Jaseng Hospital of Korean Medicine (Gangnam main branch) as part of a previous clinical study which was conducted from November, 2006 to April, 2007
  • Patients who give voluntary written informed consent to long-term follow-up assessment (quantitative and qualitative questionnaires, and MRI) at 10 years.

排除标准

  • Patients who cannot give voluntary written informed consent to this study or answer study questionnaires (e.g. severe psychological disorders)
  • Patients participating in other clinical studies or otherwise deemed unsuitable by the researchers

结局指标

主要结局

Change in Visual Analogue Scale (VAS) of radiating leg pain

时间窗: Difference from baseline at 10 years

Visual Analogue Scale (VAS) uses a 10cm line labeled at each end with scale anchors. In pain measurement using VAS, patients are asked to mark a point that represents their pain between the anchors of 'no pain (minimum score: 0)' and 'worst pain imaginable (maximum score: 100)'. Total scores are recorded in millimeters with a total range of 0-100 millimeters. Higher VAS values represent more severe pain, and a greater change from baseline (If baseline - follow up is a positive value) indicates a better outcome.

次要结局

  • Oswestry Disability Index (ODI)(Baseline, 10 years)
  • Medical history(10 years)
  • Numeric Rating Scale (NRS) of radiating leg pain(Baseline, and 10 years)
  • Patient Global Impression of Change (PGIC)(Baseline, 10 years)
  • Visual Analogue Scale (VAS) of radiating leg pain(Baseline, and 10 years)
  • Lumbar range of movement (ROM)(Baseline, 10 years)
  • Straight leg raise (SLR) test(Baseline, 10 years)
  • Adverse events(10 years)
  • Visual Analogue Scale (VAS) of low back pain(Baseline, and 10 years)
  • Numeric Rating Scale (NRS) of low back pain(Baseline, and 10 years)
  • 36-Item Short Form Survey (SF-36)(Baseline, 10 years)
  • Qualitative questionnaire on 10 year course(10 years)

研究者

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

In-Hyuk Ha, KMD

Director

Jaseng Medical Foundation

研究点 (1)

Loading locations...

相似试验