Status:
NOT_YET_RECRUITING
A Pragmatic Randomized Controlled Trial: The Efficacy and Safety of Shoulder MSAT on in Patients With Shoulder Pain
Lead Sponsor:
Jaseng Medical Foundation
Conditions:
Shoulder Pain
Eligibility:
All Genders
19-70 years
Phase:
NA
Brief Summary
This study will test the effectiveness and safety of Motion Style Acupuncture Treatment (MSAT) for shoulder pain caused by traffic accidents. About 98 hospitalized patients with acute shoulder pain af...
Detailed Description
This pragmatic randomized controlled trial is designed to evaluate the efficacy and safety of Motion Style Acupuncture Treatment (MSAT) for acute shoulder pain resulting from traffic accidents. Should...
Eligibility Criteria
Inclusion
- Adults aged 19 to 70 years
- Hospitalized with shoulder pain within 5 days after a traffic accident
- Shoulder pain intensity ≥ 5 on the Numeric Rating Scale (NRS) with observed limitation of movement
- Able and willing to provide written informed consent
Exclusion
- Serious conditions causing shoulder pain (e.g., malignant tumor, infection)
- Progressive or severe neurological deficits
- Recent shoulder surgery or procedure within 3 weeks
- Shoulder pain mainly due to non-shoulder disorders (e.g., fibromyalgia, rheumatoid arthritis, gout)
- Contraindications to MSAT (e.g., fracture, dislocation, ligament rupture or instability, severe inflammation)
- Chronic diseases interfering with assessment (e.g., cardiovascular disease, renal disease, diabetic neuropathy, dementia, epilepsy)
- Current use of steroids, immunosuppressants, psychiatric drugs, or other medications that may affect results
- Contraindications to acupuncture (e.g., bleeding disorders, anticoagulant use, severe diabetes, severe cardiovascular disease)
- Pregnant or planning pregnancy
- Severe psychiatric illness
- Participation in another interventional clinical trial
- Unable to provide informed consent
- Any other condition deemed inappropriate by the investigator
Key Trial Info
Start Date :
October 30 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
98 Patients enrolled
Trial Details
Trial ID
NCT07187336
Start Date
October 30 2025
End Date
December 31 2026
Last Update
September 23 2025
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