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Comparison of the Efficacy and Safety of Dexamethasone Palmitic Acid Injection and Compound Betamethasone Injection in Soft Tissue Interventional Therapy for Acute and Chronic Painful Diseases

Comparison of the Efficacy and Safety of Dexamethasone Palmitic Acid Injection and Compound Betamethasone Injection in Soft Tissue Interventional Therapy for Acute and Chronic Painful Diseases

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116219
Enrollment
Unknown
Registered
2026-01-07
Start date
2026-01-07
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Weichteilschmerzen

Interventions

Compound Betamethasone Injection Group:Compound Betamethasone Injection
Dexamethasone Palmitate Injection Group:Dexamethasone Palmitate Injection

Sponsors

Zhejiang Provincial Hospital of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age range: 18-80 years old, gender is not limited; 2.It meets the relevant diagnostic criteria for acute and chronic soft tissue pain diseases or neuropathic pain. Soft tissue pain diseases with a history of less than 4 weeks are defined as acute, and those with a history of 4 weeks or more are defined as chronic. Neuropathic pain with a history of >=3 months is defined as chronic; 3.The average NRS score for pain intensity in the target area is >=4 points; 4.Poor response, intolerance, or contraindications to conventional conservative treatments (such as medication, physical therapy, etc.); 5.Voluntarily participate in this study, understand the research process, and sign a written informed consent form;

Exclusion criteria

Exclusion criteria: 1.Absolute contraindications: Active infection, ulceration, or tumor at the puncture site; 2.Drug allergy: Known hypersensitivity to the investigational drugs (dexamethasone palmitate, compound betamethasone, or any excipient components) or to the local anesthetics used; 3.Severe systemic diseases: Presence of uncontrolled severe systemic conditions (e.g., heart failure, severe hepatic or renal insufficiency, uncontrolled hypertension/diabetes mellitus); 4.Coagulopathy: Significant coagulation abnormalities (INR >1.5, APTT >1.5 times the upper limit of normal, platelet count <50×10?/L), coagulopathies such as hemophilia, or current use of anticoagulant/antiplatelet medications that cannot be safely withheld for the required duration prior to the procedure. 5.Special populations: Pregnant or lactating women; 6.Cognitive and functional impairment: Severe cognitive or psychiatric disorders that preclude cooperation with evaluation and follow-up procedures; 7.Previous treatment: Having received corticosteroid injection therapy in the target area within the preceding 3 months;

Design outcomes

Primary

MeasureTime frame
numerical rating scale (NRS);Zeitraum zwischen der ersten Behandlung und dem Wiederauftreten der Schmerzen (NRS >= 4 Punkte und mindestens 24 Stunden andauernd) oder der Notwendigkeit weiterer medizinischer Ma?nahmen (wie Medikamente, Physiotherapie oder erneute Injektion);

Countries

China

Contacts

Public ContactZhang juan

Zhejiang Provincial Hospital of TCM

Zhangjuan8989@hotmail.com+86 139 5815 0569

Outcome results

None listed

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