Clinical study of electronic moxibustion on functional recovery of patients after rotator cuff repair
Not Applicable
- Conditions
- Rotator cuff injury
- Registration Number
- ITMCTR2100005402
- Lead Sponsor
- Hwa Mei Hospital, University of Chinese Academy of Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
(i) Patients with unilateral rotator cuff injury requiring arthroscopic treatment of the shoulder; (ii) All patients diagnosed by MRI, with the degree of rotator cuff tendon degeneration according to Patte's classification as type I, II or III tears; (iii) Informed consent signed by the patient; (iv) Complete follow-up of 3 months or more.
Exclusion Criteria
(i) combined glenoid labrum, subscapularis and biceps tendon injuries, glenohumeral arthritis; (ii) history of previous surgery on the affected shoulder; (iii) patients with epilepsy; congenital joint deformities and conditions that may affect recovery (e.g. paralysis, spinal deformities, autoimmune diseases, myocardial infarction, etc.)
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method visual analogue scale;
- Secondary Outcome Measures
Name Time Method Coustart-Murley score;Shoulder Range of Motion;