Trauma Wound wound dressing, pain, wound adherent, skin irritation
Conditions
Interventions
Wound dressing,Wound dressing,Wound dressing,Wound dressing,Wound dressing,Wound dressing
Experimental Device,Active Comparator Device,Active Comparator Device,Active Comparator Device,Active Comparator Device,Active Comparator Device
hydrocolloid polyester dressing,Hydrofiber dressing,hydrocolloid polyester dressing 2,soft paraffin gauze ,Foam dressing,Biocellulose dressing
Sponsors
Siriraj hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: patients who aged between 18 to 80 years old, with more than 10 cm2 in area, and had injured wound on arms or legs were recruited in this study.
Exclusion criteria
Exclusion criteria: volunteer who had a history of allergic to dressing, Herbs (Aloe vera, Centella asiatica), signs of wound infection, a previous history of chronic pain or psychotic disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain asssessment 24 hours Numeric Rating Scale | — |
Secondary
| Measure | Time frame |
|---|---|
| Dressing removal evaluation 24 hours dressing removal evaluation | — |
Countries
Thailand
Contacts
Public ContactPornprom Muangman
Faculty of Medicine Siriraj Hospital
Outcome results
None listed