Skip to main content
Clinical Trials/KCT0001850
KCT0001850
Completed
未知

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

Pusan National University Korean Medicine Hospital0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the musculo-skeletal system and connective tissue
Sponsor
Pusan National University Korean Medicine Hospital
Enrollment
60
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Pusan National University Korean Medicine Hospital

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • 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 with spinal surgery history within 3 months
  • 3\) Patients with other chronic disease(s) which may interfere with treatment effect or interpretation of outcome (e.g. chronic renal failure)
  • 4\) Patients with progressive neurologic deficit or severe neurologic symptoms
  • 5\) Patients with inner fixation or stabilization device applied through spinal surgery
  • 6\) Patients currently taking steroids, immunosuppressants, medicine for mental illness or other medication(s) that may interfere with study results
  • 7\) Patients who have received Chuna manual therapy or medicine which may influence pain levels such as nonsteroidal anti\-inflammatory drugs (NSAIDs) within the past week
  • 8\) Pregnant patients or patients with plans of pregnancy
  • 9\) Patients participating in other clinical studies or otherwise deemed unsuitable by the researchers

Outcomes

Primary Outcomes

Not specified

Similar Trials