Rotator cuff tear
Conditions
Interventions
Experimental group:5% lidocaine plaster
Sponsors
The First Affiliated Hospital of Soochow University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients aged between 18 and 80 years who have been diagnosed with rotator cuff surgery; 2. Able to understand and follow the study protocol throughout the study period and have signed a written informed consent.
Exclusion criteria
Exclusion criteria: 1. Pregnancy; 2. Patients with known allergy to lidocaine or adhesives; 3. Patients with a history of arrhythmia or myocardial infarction; 4. Irreparable tear; 5. Patients with industrial injury compensation claims or pending lawsuits.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Western Ontario Rotator Cuff Index Scores; | — |
Secondary
| Measure | Time frame |
|---|---|
| Range of motion;Visual Simulation Pain Score (resting, activity);Pressure pain threshold (PPT);American Society for Shoulder and Elbow Surgery Score;Constant Murley Score;Pittsburgh Sleep Quality Index;Oxford Shoulder Score;Simple Shoulder Test; | — |
Countries
China
Contacts
Public ContactGuo Jiongjiong
The First Affiliated Hospital of Soochow University
Outcome results
None listed