Actively Recruiting
Sodium Aescinate for the Treatment of Low Back Pain (LBP) in Adults
Led by Xijing Hospital · Updated on 2026-03-20
40
Participants Needed
1
Research Sites
182 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to assess the clinical efficacy and safety of sodium aescinate in treating low back pain (LBP) in adult participants.
CONDITIONS
Official Title
Sodium Aescinate for the Treatment of Low Back Pain (LBP) in Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with chronic low back pain lasting at least 12 weeks according to Chinese clinical guidelines
- Moderate to severe pain with a Visual Analog Scale (VAS) score greater than 4
- Aged between 18 and 65 years
- Understands the study and is willing to cooperate
- Has voluntarily signed the informed consent form
You will not qualify if you...
- Currently in acute pain phase or experiencing acute worsening of chronic pain
- Low back pain caused by infections, tumors, or other specific conditions like spinal tumors or tuberculosis
- Allergic to sodium aescinate
- Has systemic diseases or organ dysfunction
- Participated in another clinical trial within the past month
- Severe mental illness or conditions preventing cooperation
- Pregnant, breastfeeding, or planning pregnancy
- Has metal implants or other reasons making MRI unsuitable
- Considered by the researcher to be unable to complete the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Xjing hospital
Xi'an, Shaanxi, China, 710032
Actively Recruiting
Research Team
B
Bo Gao, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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