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Clinical study of electronic moxibustion on functional recovery of patients after rotator cuff repair

Clinical study of electronic moxibustion on functional recovery of patients after rotator cuff repair

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054283
Enrollment
Unknown
Registered
2021-12-12
Start date
2021-12-19
Completion date
Unknown
Last updated
2022-11-14

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

Conditions

Rotator cuff injury

Interventions

Sponsors

Ningbo Huamei Hospital, University of Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with unilateral rotator cuff injury who need shoulder arthroscopic surgery; 2. All patients were diagnosed by MRI, and the degree of rotator cuff tendon retraction was classified as type I, II, and III tears according to Patte classification; 3. The patient signs the informed consent; 4. Complete follow-up for 3 months or more.

Exclusion criteria

Exclusion criteria: 1. Combined with glenoid labrum, subscapularis muscle and biceps tendon injury, glenohumeral arthritis; 2. History of previous shoulder surgery on the affected side; 3. Epilepsy patients; 4. Congenital joint deformities, and diseases that may affect recovery (such as paralysis, spinal deformities, autoimmune diseases, myocardial infarction, etc.).

Design outcomes

Primary

MeasureTime frame
Visual analogue scale;

Secondary

MeasureTime frame
Coustart-Murley score;Shoulder range of motion assessment;

Countries

China

Contacts

Public ContactWu Wei

Ningbo Huamei Hospital, University of Chinese Academy of Sciences

244272850@qq.com+86 13738440545

Outcome results

None listed

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