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Electroacupuncture Promotes Tendon to Bone Healing and Functional Rehabilitation After Rotator Cuff Repair: A Prospective, Randomised Controlled Trial.

Electroacupuncture Promotes Tendon to Bone Healing and Functional Rehabilitation After Rotator Cuff Repair: A Prospective, Randomised Controlled Trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066443
Enrollment
Unknown
Registered
2022-12-06
Start date
2022-12-06
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Rotator cuff injury

Interventions

Control group:Conventional functional therapy
Electroacupuncture group:Electroacupuncture
Sham Electroacupuncture Group:Sham Electroacupuncture

Sponsors

Department of Bone and Joint Surgery and Sports Medicine Center, The First Affiliated Hospital, Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) All patients diagnosed with rotator cuff injury whose MRI of the shoulder joint meets the diagnostic criteria for a total rotator cuff tear (DeOrio and Cofield staging: small tears = 40 years old and < 70 years old, with full understanding, agreed to participate in this study, and had a clinical follow-up period of 36 months.

Exclusion criteria

Exclusion criteria: (1)Patient with imaging showing shoulder dislocation, fracture and cofield huge rotator cuff tear (>5cm); (2)Other shoulder diseases (such as inflammatory arthritis, frozen shoulder); (3)Previous history of surgical treatment of the ipsilateral shoulder; (4)Patients with severe osteoporosis; (5)Patients who have been treated with hormonal drugs in the 6 months before surgery; (6)Patients with a history of malignant tumor; (7)Patients whose clinical presentation cannot be evaluated; (8)Patients with local skin infection or skin ulcerations in the acupuncture area; (9)Patients with severe cardiovascular diseases; (10)Patients with pacemakers; (11)Patients who are planning to become pregnant, pregnant or lactating; (12)Patients who cannot tolerate electroacupuncture treatment; (13)Other patients who are judged by the investigator or assistant investigator to be unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
Tendon to bone healing;

Secondary

MeasureTime frame
Visual analogue scale(VAS);Range of Motion(ROM);American Shoulder and Elbow Surgeons(ASES);University of California at Los Angeles(UCLA);Shoulder Pain and Disability Index(SPADI);Short form 36 questionnaire;Adverse events;

Countries

China

Contacts

Public ContactHuajun Wang

Department of Bone and Joint Surgery and Sports Medicine Center, The First Affiliated Hospital, Jinan University, Guagzhou

30442372@qq.com+8618026278776

Outcome results

None listed

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