Effectiveness of Joins® for Managing Lumbar Facetogenic Pain: A Prospective, Randomized, Double-blind, Placebo-controlled, Pilot Study

2309-118-1470

Obtain informed consent from patients with lumbar facet joint syndrome and, after enrollment, randomly assign them to Group A (Joins®) or Group B (Placebo). According to the allocation in each group, participants are instructed to take Joins® 200mg 1 tablet three times a day or placebo 1 tablet three times a day from day 1. Research subjects visit at 4-week intervals a total of 3 times (4 weeks, 8 weeks, 12 weeks) to collect various measurement variables. Both the test and control groups are observed during the period of taking the investigational medication without any changes or additional facet joint-related procedures (medial branch block, facet joint block). Acetaminophen is allowed as a rescue medication.

2024-06-22

2026-01-20

2026-04-20

Not yet recruiting

76

Inclusion Criteria: 1. Adults between 19 and 80 years of age 2. Those diagnosed with lumbar facet joint syndrome through diagnostic posterior medial limb block 3. Those with an average 11-point numeric rating scale (NRS) of 4 or more for back pain over the past 24 hours 4. Those who voluntarily decided to participate in the study and gave written consent Exclusion Criteria: 1. Patient refusal 2. If the main cause of the current back pain is infectious spondyloarthrosis/arthropathy, ankylosing spondylitis, or stenosis, or if the patient complains or shows signs of local neurological symptoms (e.g., decreased motor power in the lower extremities) due to the underlying disease. 3. Patients with moderate to severe lumbar instability requiring surgery 4. Cognitive decline to the point where the numeric pain rating (NRS) cannot be understood. 5. Severe cardiovascular disease (Systolic BP \>=160 mm Hg or diastolic BP \>=100 mm) or liver (AST/APT increased more than twice normal) or kidney disease (GFR\<60 mL/min/1.73 m2) A person with teeth 6. Those with systemic infection or spinal infection 7. Those who are allergic to clinical trial drugs or their ingredients 8. People with genetic problems such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption 9. If you are pregnant or breastfeeding. For women of childbearing potential, those who are unwilling to use a reliable method of contraception during the administration period and for more than 4 weeks after the last administration of the investigational drug * Women who have had menarche and have not reached postmenopausal status (≥12 months of consecutive amenorrhea without an identified cause other than menopause) and who have not undergone surgical sterilization (ovarian and/or hysterectomy) are considered women of childbearing potential. * You must remain abstinent (abstain from sexual intercourse with the opposite sex) or use two medically acceptable forms of contraception. One method of contraception with a low failure rate, defined as less than 1% per year (e.g., oral contraceptives or intrauterine device), and a medically acceptable second method, such as spermicide and condom use by the male partner, should be used. Barrier methods alone are not permitted. Male subjects should use condoms and spermicides during sexual intercourse, and female contraceptive partners should also be careful to use at least one additional method of contraception with a low failure rate as defined above. * The reliability of sexual abstinence must be evaluated considering the clinical trial period and the test subject's preferred daily lifestyle habits. Periodic abstinence (e.g., date, ovulation, symptom-temperature, or post-ovulation abstinence) and external ejaculation are not acceptable methods of contraception. 10. Those with malignant tumor in the lumbar region 11. Those who have previously undergone lumbar surgery or are scheduled to undergo spine surgery within 12 weeks after screening 12. Subjects who participated in other clinical trials within 6 months before the first administration of the investigational drug 13. Other people who are not suitable for this clinical trial according to the researcher's judgment

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2024-05-29