Overview
This is a non-inferiority randomized controlled trial, recruiting 150 patients with chronic non-specific low back pain. The patients will be randomly assigned either to Yanqing Zhitong Ointment acupoint application group (Treatment Group) or the acupuncture group (Control Group) in a 1:1 ratio.
Description
This is a non-inferiority randomized controlled trial, 150 patients with chronic non-specific low back pain were randomly assigned to acupoint application group and acupuncture group in a 1:1 ratio. The main acupoints are Ashi points, Shenshu(BL23), Guanyuanshu(BL26). The primary outcome measure is the change of McGill Pain Questionnaire (MPQ) before and after treatment.
Eligibility
Inclusion Criteria:
- Diagnosed with non-specific low back pain
- Aage from 18 to 65
- VAS between 4 and 7
- No other treatment in the past 3 months
- No other simultaneous relevant treatment
- Voluntarily joining this study with informed consents
Exclusion Criteria:
- Pregnant women
- With skin ulcers or contusion wounds
- Past history of severe allergy to transdermal preparations
- Complicated with serious diseases