drugset / Trial / NCT02384928

Effects of Shinbaro Pharmacopuncture in Sciatic Pain Patients With Lumbar Disc Herniation

NCT02384928

Completed 60 enrolled Jaseng Medical Foundation
RandomizedParallel-groupTriple-blindTreatment

Summary

This trial will evaluate the comparative clinical effectiveness of pharmacopuncture for severe non-acute sciatic pain patients diagnosed with lumbar disc herniation (LDH) with usual care of conventional medicine and that of Korean medicine (acupuncture). Sixty patients with severe non-acute sciatic pain patients diagnosed with LDH (NRS ≥5, 4 weeks - 6 months) will be recruited, and randomized 20 each to the Shinbaro pharmacopuncture, acupuncture, and usual care group, respectively. The 2 acupuncture groups will receive 2 sessions/week of acupuncture alone or with pharmacopuncture for 4 weeks, and the usual care group will receive conventional medication 2 times/day and 2 sessions/week of physical therapy. Post-treatment evaluations will take place 5, 7, 9, and 12 weeks after randomization.

Timeline

Start
2015-09-09
Primary completion
2017-01-31
Completion
2017-03-16

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aceclofenac Small molecule
Comparator Diclofenac Other / unclassified
Comparator Loxoprofen Small molecule
Comparator Talniflumate Small molecule
Comparator Tramadol Other / unclassified