Comparison of the effects of PRP injection of supraspinatus tendon and acromial sac and PRP injection of acromial sac in partial rotator cuff injury

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900027472

Enrollment

Unknown

Registered

2019-11-14

Start date

2019-11-30

Completion date

Unknown

Last updated

2019-11-18

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

Conditions

rotator cuff injury

Interventions

Experimental group:???

control group:???

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Pain in the front triangle of the shoulder joint. 2. The history of onset is 150 000/ml. 6. Aged > 18 and < 60 years. 7. The patient has not received relevant treatment within 3 months. 8. The patient has signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. The patient has rheumatoid arthritis, ankle arthritis, biceps long-headed keyhole effusion, full rotator cuff tear, fracture, infection or tumor. 2. The patient has unstable angina, mental illness, and mental illness. 3. The shoulder joint has undergone rotator cuff repair surgery. 4. Passive joint mobility loss exceeds 20%. 5. Fat infiltration more than 50%. 6. Suffering from vascular insufficiency, muscle atrophy or neurological disease. 7. Have been pregnant or have a birth plan for nearly 1 year.

Design outcomes

Primary

Measure	Time frame
VAS;UCLA;	—

Secondary

Measure	Time frame
MRI;Ultrasonography;	—

Countries

China

Contacts

Public ContactZishan Jia

Orthopedics Department, General Hospital of PLA

jzs1963@163.com+86 15210889919

Outcome results

None listed

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