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Ultrasound-guided leukocytes-poor platelet-rich plasma injection for lateral epicondylitis, a randomized, double-blinded, controlled trial

Ultrasound-guided leukocytes-poor platelet-rich plasma injection for lateral epicondylitis, a randomized, double-blinded, controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024425
Enrollment
Unknown
Registered
2019-07-11
Start date
2019-09-01
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

lateral epicondylitis

Interventions

Leukocyte-poor PRP group:Leukocyte-poor-platelet-rich plasma
NS group:saline solution

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Diagnosed with lateral epicondylitis over 3 months, suffering from pain with VAS (visual analog scale) >= 5, aged 18 to 65 years, ultrasonographic confirmation of lateral epicondylitis.

Exclusion criteria

Exclusion criteria: Patients with immune system diseases or neurological disorders, such as cervical radiculopathy or carpal tunnel syndrome, peripheral nerve injury; affected upper arm with elbow or wrist fractures; patients with a history of elbow surgery; taking oral NSAIDs medication within last 2 weeks or local steroid injections within last 6 weeks; patients with history of allergy reaction, cardiopulmonary insufficiency, thrombocytopenia or other coagulation disorder; pregnant females; patients with tumor or those who can complete this trial.

Design outcomes

Primary

MeasureTime frame
ASES score;

Secondary

MeasureTime frame
Quick DASH (Disabilities of the Arm, Shoulder, Hand);VAS score;

Countries

China

Contacts

Public ContactHe Hongchen

West China Hospital, Sichuan University

912606137@qq.com+86 18980602262

Outcome results

None listed

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