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A Comparative Study on the Clinical Efficacy of PRP Combined with Scapular Stabilization Training in the Treatment of Rotator Cuff Injuries: An Assessment Based on Ultrasound Elastography

A Comparative Study on the Clinical Efficacy of PRP Combined with Scapular Stabilization Training in the Treatment of Rotator Cuff Injuries: An Assessment Based on Ultrasound Elastography

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120497
Enrollment
Unknown
Registered
2026-03-16
Start date
2026-03-16
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Rotator Cuff Injury

Interventions

Training Group:Scapular stabilization training alone combined with physical modality therapy.
PRP Group:PRP injection alone combined with physical modality therapy.
Combination Group:PRP injection combined with scapular stabilization training and physical modality therapy.

Sponsors

Yibin Hospital Of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of the *Guidelines for the Diagnosis and Treatment of Rotator Cuff Injuries (2022 Edition)* and be diagnosed with mild-to-moderate injury (partial-thickness tendon tear, with tear extent <= 50% of tendon thickness) via ultrasound/MRI; 2. Aged 35–70 years; 3. Have not received any rotator cuff-related treatments (e.g., PRP, steroid injections, surgery) in the past 3 months; 4. Able to comply with the 8-week treatment and 24-week follow-up; 5. Provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Complete rotator cuff tear, shoulder joint infection, fracture, or tumor; 2. Coagulation disorders or autoimmune diseases; 3. Severe cardiac, hepatic, or renal diseases, or cognitive impairment; 4. Pregnancy or lactation; 5. Concurrent participation in other similar studies.

Design outcomes

Primary

MeasureTime frame
pain intensity;shoulder range of motion;shear wave elastography value measurement;

Secondary

MeasureTime frame
shoulder function;

Countries

China

Contacts

Public ContactFeng Wang

Yibin Hospital Of Traditional Chinese Medicine

312779971@qq.com+86 173 1322 4651

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026