None listed
Conditions
Interventions
Others(Comparison between herbal medicine strategy and conventional Korean medicine treatment) : Experimental group: A strategy to take herbal medicine prescriptions that do not limit the type and do
Sponsors
Kyung Hee University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) 19 years of age or older, relevant male/female 2) If a disc swelling abnormality is observed in the lumbar area on MRI or CT and there is a radiating pain symptom consistent with it 3) In the NRS indicators, no more than 3 and no more than 6, lower limb radiating pain 4) Patients who agreed to participate in the clinical study and provided written consent to the test subjects
Exclusion criteria
Exclusion criteria: 1) Patients with congenital deformities in the lumbar spine or within 3 months after lumbar surgery 2) If there is a red signal that may suspect Mami's syndrome, such as urination disorder, defecation disorder, or decreased sensation in the bone hemisphere 3) When a concomitant disease such as tumor, fracture, infection, etc. is observed in the lumbar spine 4) In the case of direct injection treatment including steroid in the lumbar spine within one week 5) If you are being treated for a mental illness such as depression or schizophrenia 6) If you have other conditions that may interfere with treatment, such as severe gastrointestinal disease, cardiovascular disease, high blood pressure, diabetes, kidney disease, liver disease, thyroid dysfunction, etc 7) A person who is pregnant or breastfeeding, or who has a pregnancy plan 8) Inadequate or unsafe acupuncture treatment: Severe diabetic patients with hemorrhagic disease, risk of infection 9) Inadequate or unsafe treatment of herbal medicines: those who have a disease that may affect drug use or absorption, those who have digestive problems after surgery related thereto, those who receive anticoagulant therapy, or who have severe liver or kidney disease (AST, ALT, ?-GTP, serum creatine are more than twice the upper limit of normal screening) 10) Participation in other clinical studies has not been completed within one month, or participation in other clinical studies is planned within six months from the date of selection 11) If it is difficult to write a consent form for participation in the study 12) If it is difficult for the researcher to participate in the clinical study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| numeral rating scale(NRS)_radiating pain;Oswestry disability Inventory (ODI) | — |
Secondary
| Measure | Time frame |
|---|---|
| visual analog scale (VAS);Roland-Morris disability questionnaire (RMDQ);EuroQol-5 Dimension-5 Level (EQ-5D-5L);Health-related Quality of Life Instrument with 8 Items (HINT-8);Global Perceived Effect (GPE);Patient Health Questionnaire-15 (PHQ-15);vital signs;a physical measurement;clinical laboratory examination;an abnormal reaction;numeral rating scale(NRS)_low back pain | — |
Countries
Korea, Republic of
Contacts
Public ContactJung-Hyun Kim
Kyung Hee University Oriental Medicine Hospital at Gangdong
Outcome results
None listed