Non-infected wounds and full skin thickness.
Conditions
Interventions
Intervention 1: Control group: The recipient group is a type of commercial hydrogel scaffold available in the market. Intervention 2: Intervention group 1: The group receiving pectin/chitosan/polyviny
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Adults aged 18 to 65 years with non-infected, full-thickness wounds
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The result of using the relevant hydrogel is wound healing, which can be tracked and traced through the follow-up every two days of the people who have used the relevant hydrogel for wound healing. Timepoint: The examination is evaluated on days 7, 14 and 21 and until full recovery. Method of measurement: Inspection is done by digital camera. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactfereshteh nejaddehbashi
Ahvaz University of Medical Sciences
Outcome results
None listed