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Shoulder joint Rotator cuff injury: A study on the efficacy of electroacupuncture based on hemodynamics in promoting rehabilitation after rotator cuff repair surgery

Shoulder joint Rotator cuff injury: A study on the efficacy of electroacupuncture based on hemodynamics in promoting rehabilitation after rotator cuff repair surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002542
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-12-25
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Rotator cuff injury

Interventions

Treatment group:Electroacupuncture Combined with Basic Rehabilitation Training

Sponsors

Shanghai Sixth People's Hospital Affiliated to Shanghai JiaoTong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 40~75 years, gender; 2. Symptoms and signs Clinical Practice Guidelines for Rotator Cuff Injuries by the American Academy of Orthopaedic Surgeons; 3. Preoperative diagnosis of rotator cuff tear via MRI, with Ellman classification of <5 cm full-thickness tear (including supraspinatus, infraspinatus, and teres minor), confirmed arthroscopically during surgery; 4. Undergoing ARCR for a single-sided rotator cuff (as ARCR is typically performed alongside other procedures, such as subacromial decompression and distal clavicle resection, to enhance generalizability in this study, patients' ARCR surgery may be combined with these procedures); 5. Voluntarily participating in this study, willing to undergo examinations, treatments, and follow-up visits.

Exclusion criteria

Exclusion criteria: 1. Patients with shoulder pain and restricted shoulder joint movement caused by cervical disc herniation, shoulder joint tumors, shoulder dislocation, fractures, or glenohumeral lesions; 2. Patients with a torn rotator cuff, specifically a tear of the subscapularis tendon; 3. Patients with a history of shoulder or neck surgery; 4. Patients excluded if the contralateral shoulder has a rotator cuff tear, shoulder arthritis, fractures, labral injuries, or other conditions that preclude them from serving as healthy controls; 5. Patients with severe primary diseases of the heart, liver, kidneys, hematopoietic system, endocrine system, immune system, or nervous system; severe osteoporosis; tumors; or mental illness; 6. Patients with a history of alcohol or narcotic drug abuse or pain management with opioid medications; 7. Patients with allergies to acupuncture needles, local skin diseases, ulcers, infections, needle syncope, or blood disorders (e.g., coagulation disorders or bleeding disorders).

Design outcomes

Primary

MeasureTime frame
Constant Murley shoulder function score;

Secondary

MeasureTime frame
The time for CMS to reach the minimal clinically important difference (MCID);Shoulder joint active range of motion;Western Ontario Rotator Cuff Index;Pain visual analogue scale;Response Rate;Magnetic Resonance Image;

Countries

China

Contacts

Public ContactZhao jinzhong

Shanghai Sixth People's Hospital Affiliated to Shanghai JiaoTong University

zhaojinzhong@vip.163.com+86 189 3017 4920

Outcome results

None listed

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