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临床试验/KCT0002329
KCT0002329进行中(未招募)未知

Clinical research of Comparative Effectiveness and Cost-effectiveness of Chuna manual therapy for non-acute Low back pain : Multi-center Randomized Controlled Trial

Pusan National University Korean Medicine Hospital0 个研究点目标入组 194 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
194

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 70(Year)(—)
性别
All

入选标准

  • 1) Non-acute low back pain patients (with pain duration of 3 weeks or longer) with average Numeric Rating Scale (NRS) =5 during the past week
  • 2) Patients aged 19 years or older and 70 years or younger
  • 3) Patients who have agreed to trial participation and provided written informed consent

排除标准

  • 1) Patients diagnosed with serious pathology(s) which may cause low back pain (e.g. spinal metastasis of tumor(s), acute fracture, spinal dislocation)
  • 2) Patients who are suspected of fracture according to the researcher's clinical judgment
  • 3) Patients with spinal surgery history within 3 months
  • 4) Patients with other chronic disease(s) which may interfere with treatment effect or interpretation of outcome (e.g. chronic renal failure)
  • 5) Patients with progressive neurologic deficit or severe neurologic symptoms such as cauda equina syndrome
  • 6) Patients with inner fixation or stabilization device applied through spinal surgery
  • 7) Patients currently taking steroids, immunosuppressants, medicine for mental illness or other medication(s) that may interfere with study results
  • 8) Patients who have received Chuna manual therapy, medicine such as nonsteroidal anti-inflammatory drugs (NSAIDs), or invasive treatments such as acupuncture or injections within the past week
  • 9) Pregnant patients, breastfeeding patients or patients with plans of pregnancy
  • 10) Patients participating in other clinical studies or otherwise deemed unsuitable by the researchers
  • 11) Patients who received surgery, procedures or medication treatment that may interfere with study results during the intervention period (7 weeks) without consulting with the attending physician

研究者

发起方
Pusan National University Korean Medicine Hospital

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