Acupoint Application With Yanqing Zhitong Ointment for Chronic Non-specific Low Back Pain
Active, not recruitingNot applicableNCT06102291
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
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.
Study details
- Official title
- Effect of Acupoint Application With Yanqing Zhitong Ointment for Chronic Non-specific Low Back Pain: a Non-inferiority Randomized Controlled Trial
- Conditions
- Non-specific Low Back Pain
- Interventions
- Other: Yanqing Zhitong Ointment Acupoint application
- Other: Acupuncture
- Sponsor
- ZhanYJ
- Organization
- Shanghai University of Traditional Chinese Medicine
- Start date
- 2022-07-01
- Primary completion
- 2026-04-30
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- China
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Diagnosed with non-specific low back pain 2. Aage from 18 to 65 3. VAS between 4 and 7 4. No other treatment in the past 3 months 5. No other simultaneous relevant treatment 6. Voluntarily joining this study with informed consents Exclusion Criteria: 1. Pregnant women 2. With skin ulcers or contusion wounds 3. Past history of severe allergy to transdermal preparations 4. Complicated with serious diseases
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06102291