post-operative wound
Conditions
Interventions
none
Sponsors
Department of Dermatology Gunma graduate school of medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patient: 20 years old<= 2) Post-operative wound or early pressure ulcer 3) Patients who agreed with this study by written informed consent
Exclusion criteria
Exclusion criteria: 1) Patients who have allergy to the material 2) Others 3) Patients with infection 4) Patients with deep ulcer, such as necrotic tissue
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety of the new dressing material (check contact dermatitis and infection) | — |
Secondary
| Measure | Time frame |
|---|---|
| Effectiveness of the new dressing material (by evaluation of depth, exudation, size, infection, granulation, necrotic tissue and pocket) | — |
Countries
Japan
Contacts
Public ContactAkira Shimizu
Gunma University Hospital Department of Dermatology
Outcome results
None listed