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Prospective cohort study on the treatment of chronic musculoskeletal pain with Bulleyaconitine A Tablets

Prospective cohort study on the treatment of chronic musculoskeletal pain with Bulleyaconitine A Tablets

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097021
Enrollment
Unknown
Registered
2025-02-11
Start date
2025-02-28
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Chronic musculoskeletal pain

Interventions

exposed group (Bulleyaconitine A Tablets:NA
Non-exposed group (Duloxetine hydrochloride enteric coated capsules):NA

Sponsors

The Third Affiliated Hospital of Beijing University of Chinese Medicine/Hebei Medical University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for chronic musculoskeletal pain; 2. Meet the diagnostic criteria for chronic lower back pain; 3. The most painful VAS score within 24 hours before enrollment is = 4 points; 4. Age >= 18 years old;

Exclusion criteria

Exclusion criteria: 1. Excluding those who are allergic or contraindicated to Bulleyaconitine A Tablets and Duloxetine hydrochloride enteric coated capsules; 2. Pregnant and lactating women are prohibited from using it; 3. Excluding primary diseases such as severe cardiovascular, cerebrovascular, liver, kidney, hematopoietic system, tumors, and psychiatric patients

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
Oswestry(ODI);ID Pain;EQ-5D-5L;Quantitative grading of clinical symptoms/syndromes;Pain rebound rate during follow-up period;

Countries

China

Contacts

Public ContactChen Weiheng/Hou zhiyong

The Third Affiliated Hospital of Beijing University of Chinese Medicine/HEBEI MEDICAL UNIVERSITY THIRDHOSPITAL

drchenweiheng@163.com+86 10 5207 5271

Outcome results

None listed

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