rotator cuff injury
Conditions
Interventions
control group :using conventional adhesive dressing (Cosmopor E Steri1)
experimental group:using a trial dressing (Allevyn Gentle Border Foam Dressing)
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: (I)Aged 18 ~ 80 years old; (II) initial rotator cuff repair; (III) rotator cuff repair with the same method (surgical methods, suture methods and suture materials are the same); (IV) good patient compliance and ability to complete follow-up regularly; (V) voluntary participation in the study, signed informed consent.
Exclusion criteria
Exclusion criteria: (I)combined with hypertension, diabetes, hypoproteinemia, malnutrition (BMI 28 kg/m2), rheumatoid disease, tumor, connective tissue disease, hemophilia, limb vascular disease, psoriasis, radiation injury, gangrene, genetic diseases, anemia, gout, and other diseases that may affect wound healing; (II) long-term use of immunosuppressive agents, glucocorticoids, biological agents, anticoagulants, antiplatelet drugs, and preoperative no standardized adjustment and withdrawal; (III) long-term smoking or drinking history; (IV) history of surgery or infection at the surgical site; (V) scar, skin lesion, rash at surgical site prior to surgery; (VI) Invasive procedures such as acupuncture, small needle knife, and drug injection at the surgical site recently (within 1 month); (?) patients with psoriasis, eczema or dermatitis and other skin diseases; (?) allergic to any dressing components.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the incidence rate of wound complications; the cost-effectiveness of wound care; | — |
Secondary
| Measure | Time frame |
|---|---|
| the wound healing rate; the wound healing time;dressing wear time; number of dressing changes;evaluation of dressing performance; | — |
Countries
China
Contacts
Public ContactPeng-cheng Li
West China Hospital, Sichuan University
Outcome results
None listed