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Effect of extracorporeal shock wave combined with autologous platelet-rich plasma injection on rrotator cuff calcific tendinitis: a prospective clinical study

Effect of extracorporeal shock wave combined with autologous platelet-rich plasma injection on rrotator cuff calcific tendinitis: a prospective clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084019
Enrollment
Unknown
Registered
2024-05-09
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

calcific tendinitis of the rotator cuff

Interventions

Extracorporeal shock wave group:In the shoulder pain points, choose 2 to 3 of them for each treatment, apply the coupling agent, which is convenient for the treatment head to stick to the skin, and co
Platelet-rich plasma injection group:Autologous PRP injection was performed under ultrasound guidance
ESW+PRP:Extracorporeal shock wave therapy followed by PRP injection

Sponsors

Chengdu Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for rotator cuff calcific tendonitis, aged between 40 and 60 years old (2) Persistent pain in the affected shoulder, with obvious tenderness under the acromion and rotator cuff, as confirmed by X-ray and CT and MRI examination showed one or more round-shaped high-density calcium salt deposits near the greater tuberosity of the humerus; (3) All were diagnosed for the first time; (4) Complaints of severe pain in the shoulder joint, obvious pain at night, non-steroidal anti-inflammatory drugs Drugs and other conservative treatments are not effective.

Exclusion criteria

Exclusion criteria: (1) Combined with rotator cuff trauma, long head of biceps tendonitis and other shoulder joint diseases; (2) Past combined history of shoulder joint surgery; (3) Patients with internal fixation of the shoulder joint; (4) Shoulder joint combined with infection, Tumors and other lesions; (5) Combined with severe heart, liver, and kidney dysfunction; (6) Do not agree to participate in the study or fail to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale,VAS;

Secondary

MeasureTime frame
American Shoulder and Elbow Surgeon’s Form,ASES;Constant-Murley Shoulder Score,CMS;the university of California at Los Angeles shoulder rating scale, UCLA;The location and size of the calcifications were examined by ultrasound;

Countries

China

Contacts

Public ContactXiali Xue

Chengdu Sport University

390231882@qq.com+86 184 8363 8915

Outcome results

None listed

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