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A Prospective, Observational, Multicenter Clinical Study of Yunnan Baiyao Ointment for the Treatment of Musculoskeletal Pain

A Prospective, Observational, Multicenter Clinical Study of Yunnan Baiyao Plaster for the Treatment of Musculoskeletal Pain.

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025002208
Enrollment
Unknown
Registered
2025-11-17
Start date
2025-11-20
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal pain

Interventions

Exposure group:Yunnan White Medicine Ointment
The non-exposure group:conventional therapy

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1: (1) Age = 18 years, gender; 2: (2) Meet the diagnostic criteria for musculoskeletal pain, including osteoarthritis, low back pain (including nonspecific low back pain, spine-related low back pain), cervical spondylosis, rotator cuff injury, periarthritis of the shoulder, lateral epicondylitis of the humerus (tennis elbow), medial epicondylitis of the humerus (golfer's elbow), and chronic pain after musculoskeletal injury; 3: (3) Persistent or intermittent pain = 30 days, with no indication for surgery; 4: (4) Volunteers who sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1: (1) Generalized pain, cancer-related pain, neuropathic pain (such as herpes zoster and postherpetic neuralgia, diabetic neuropathy, complex regional pain syndrome, postoperative pain syndrome, phantom limb pain, central pain), vascular pain (such as erythromelalgia, acrocyanosis, atherosclerotic occlusive disease, thromboangiitis obliterans, Raynaud's disease, thrombophlebitis, livedo reticularis, giant cell arteritis, etc.), and rheumatic immune diseases (such as rheumatoid arthritis, ankylosing spondylitis, etc.). 2: (2) History of neurological and psychiatric diseases, such as schizophrenia, depression, epilepsy, or acute episodes of epilepsy, or long-term use of psychiatric medications. 3: (3) Concurrent malignant tumors, severe primary cardiovascular diseases (cardiovascular diseases with significant clinical symptoms and potential severe complications), severe liver or kidney diseases, or other serious conditions affecting survival. 4: (4) Individuals with damaged or abnormal skin at the application site (such as rashes, eczema, post-surgery, etc.), or individuals with allergic skin conditions. 5: (5) History of allergy to the patch matrix or investigational drug, or allergic constitution (allergic to two or more substances). 6: (6) Pregnant women, breastfeeding women, or those with recent plans for pregnancy. 7: (7) Participants who have been involved in other interventional clinical trials within the past three months. 8: (8) Individuals deemed unsuitable for participation in the study by the investigator, such as those with physical or work conditions that may exacerbate pain.

Design outcomes

Primary

MeasureTime frame
EuroQoL Five-Dimensional Questionnaire;Pain NRS Score;Anxiety and Depression Scale;

Countries

China

Contacts

Public ContactXiao Hong

West China Hospital of Sichuan University

xiaohonghuaxi@126.com18980601980

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026