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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
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100005402
Enrollment
Unknown
Registered
2021-12-12
Start date
2021-12-19
Completion date
Unknown
Last updated
2023-02-20

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

Hwa Mei Hospital, University of Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

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

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.)

Design outcomes

Primary

MeasureTime frame
visual analogue scale;

Secondary

MeasureTime frame
Coustart-Murley score;Shoulder Range of Motion;

Countries

China

Contacts

Public ContactWei Wu
244272850@qq.com13738440545

Outcome results

None listed

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