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A prospective randomized controlled study of different interventional treatment methods on pain and functional recovery after shoulder arthroscopy with rotator cuff injury

A prospective randomized controlled study of different interventional treatment methods on pain and functional recovery after shoulder arthroscopy with rotator cuff injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062057
Enrollment
Unknown
Registered
2022-07-21
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Rotator cuff injury

Interventions

Autologous PRP therapy:Autologous PRP 10mL was injected 1 day before discharge and 3 weeks after discharge after arthroscopic shoulder repair, a total of two times
corticosteroid treatment group:Two injections of betamethasone (Deproxone) 5 mg/1 mL + ropivacaine 2 mL + saline 7 mL for a total of 10 mL mixture 1 day before discharge and 3 weeks after discharge af
saline control group:1 day before discharge and 3 weeks after discharge after arthroscopic shoulder repair, inject 10 mL of normal saline twice in total

Sponsors

Wang Rui
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Aged between 18-75 years old, no history of systemic or metabolic diseases; symptoms such as rotator cuff injury (including synovitis, rotator cuff tendinopathy, rotator cuff tear) and recent magnetic resonance examination (MRI) ) was confirmed; pain after arthroscopic rotator cuff repair within the last three months; no neuromuscular disease or other disorders that may affect muscle structure and echo; no family history of disease.

Exclusion criteria

Exclusion criteria: Less than 18 years of age; patients with shoulder pain without rotator cuff injury; previous non-invasive treatment, including treatment with NSAIDs and PRP and/or regular exercise and/or physical therapy for at least 2 months (TENS, ultrasound, etc.); allergic reactions to disinfectants, anesthetics, sodium citrate, and calcium chloride, etc.; thrombocytopenia, acute and chronic infections, anticoagulant therapy, etc.; previous adverse reactions to local injections (hypertension, systemic allergy, and hypersensitivity reactions), or even severe kidney or liver disease, etc.); pregnancy, malignancy, etc. within 6-12 weeks after minimally invasive treatment; patients with severe osteoporosis near the joints; patients who cannot maintain follow-up or provide informed consent.

Design outcomes

Primary

MeasureTime frame
Constant-Murley,constant;

Secondary

MeasureTime frame
visual analogue scale,VAS;University LosAngeles,UCLA scoring system;Common Terminology Criteria for Adverse Events,CTCAE;two-dimensional ultrasound;MRI;

Countries

China

Contacts

Public ContactZhang Qiang
301zq@live.cn+86 13552070988

Outcome results

None listed

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