Long Term Follow-Up of Post Neck Pain Patients Accompanying Ossification of Posterior Longitudinal Ligament Treated With Integrated Complementary and Alternative Medicine: Observational Study

  • STATUS
    Recruiting
  • participants needed
    100
  • sponsor
    Jaseng Medical Foundation
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Updated on 16 February 2024
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Summary

The purpose of this study is to reveal the effectiveness and safety of integrative Korean medicine for Ossification of Posterior Longitudinal Ligament(OPLL) by observation inpatients treated with integrative Korean medicine.

This study is a prospective observational study. The subjects for study are patients diagnosed with OPLL and who have been admitted to four Jaseng Hospital of Korean medicine (Gangnam, Bucheon, Daejeon, and Haeundae) for 2016.04.01-2019.12.31.

Medical records of selected patients will be analyzed, and telephone surveys will be conducted for each patient. The survey questions are Numeric ratinc scale (NRS), Vernon-Mior Neck Disability Index (NDI), quality of life, and Patient Global Impression of Change (PGIC), etc.

Details
Condition Medicine, Korean Traditional, Ossification of Posterior Longitudinal Ligament
Age 100years or below
Treatment phone survey
Clinical Study IdentifierNCT04446221
SponsorJaseng Medical Foundation
Last Modified on16 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

Patients diagnosed with OPLL by C spine X-ray or MRI or CT
Paithents who was admitted to Jaseng hospital of Korean medicien
Patients have agreed to participate the study

Exclusion Criteria

Patient hospitalized under 3 days
Patients who have been diagnosed with certain serious diseases that may cause disturbance to interpretation of conclusion (cardiovascular problems, kidney disease, diabetic neuropathy, dementia, epilepsy, and so on)
Patients who have been diagnosed with certain serious diseases that may cause back pain or neck pain (tumor metastases to the spine, fibromyalgia, rheumatoid arthritis, gout, and so on)
Patients had cervical spinal surgery within 3 months
Patients diagnosed with C spine fracture by C spine X-ray or MRI or CT
Patients deemed unable to participate in the clinical research by other researchers
Patients haven't agreed to participate the study
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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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