Rotator cuff tear
Conditions
Interventions
Experimental group:Intraarticular injection of Deprospan1ml
Control group:Intraarticular injection of 1 ml of normal saline
Sponsors
WestChina hospital, Sichuan university
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: (1) Rotator cuff full-thickness tear live Elman III partial tear; (2) Arthroscopic double-row suture; (3) Age 18-65;
Exclusion criteria
Exclusion criteria: (1) Patients with giant rotator cuff tears; (2) Obvious shoulder joint stiffness before surgery; (3) Shoulder instability, severe shoulder osteoarthritis, rheumatoid arthritis, tumors, infections, tuberculosis, etc.; (4) Distal clavicle resection is required; (5) History of previous shoulder surgery; (6) Have received intra-articular injection treatment (glucocorticoids, sodium hyaluronate, PRP, etc.) within half a year before surgery;(7) Other diseases that are contraindicated or not suitable for glucocorticoids, or have a history of glucocorticoid allergy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain assessment scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Rotator cuff healing;Shoulder range of motion;Shoulder function;EQ-5D; | — |
Countries
China
Contacts
Public ContactXin Tang
West China Hospital, Sichuan University
Outcome results
None listed