Long Term Follow up of Spinal Stenosis Inpatients Treated With Korean Integrative Medicine Treatment.

  • STATUS
    Recruiting
  • participants needed
    724
  • sponsor
    Jaseng Medical Foundation
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Updated on 19 February 2024
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spinal stenosis
stenosis

Summary

The purpose of this study is to reveal the effectiveness and safety of integrative Korean medicine for spinal stenosis by observation inpatients treated with integrative Korean medicine.

This study is a prospective observational study. The subjects for study are patients diagnosed with spinal stenosis and who have been admitted to four Jaseng Hospital of Korean medicine (Gangnam, Bucheon, Daejeon, and Haeundae) for 2015.01-2018.12.

Medical records of selected patients will be analyzed, and telephone surveys will be conducted for each patient. The survey questions are Numeric rating scale (NRS), Oswestry disability index (ODI), quality of life, and Patient Global Impression of Change (PGIC), etc.

Details
Condition Medicine, Korean Traditional, Spinal Stenosis Lumbar
Age 100 years and younger
Treatment phone survey
Clinical Study IdentifierNCT04443738
SponsorJaseng Medical Foundation
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

Patients diagnosed with spinal stenosis by an Korean medicine doctor and was admitted to Jaseng hospital of Korean medicien
Patients undergone MRI readings of central spinal stenosis
Patients have no communication problems
Patients have agreed to participate the study

Exclusion Criteria

Patients who have been diagnosed with certain serious diseases that may cause back pain or neck pain (tumor metastases to the spine, acute fractures, spinal dislocations, and so on)
Patient hospitalized for pain caused by a traffic accident
Patients with serious mental illness
Patients deemed unable to participate in the clinical research by other researchers
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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