Diabetic foot ulcer.
Conditions
Interventions
Intervention 1: Intervention group 1: In this group, patients will receive standard treatments plus chitosan film. * Intervention group 2: In this group, patients will receive standard treatments plus
Sponsors
Abadan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: History of type 1 or type 2 diabetes mellitus Has a Wagner grade 1 or 2 diabetic foot ulcer Age between 18-75 years Able to attend all follow-up visits
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| . Timepoint: . Method of measurement: .;The primary outcome variable in this study is the percentage of diabetic foot ulcer healing during the intervention period. This quantitative variable will be determined by measuring the wound area at specific time intervals (weekly) and calculating the percentage reduction compared to the initial wound area. The percentage of wound healing in each group at different time points will be compared using appropriate statistical methods. Timepoint: Measurements will be taken at baseline (start of treatment), 2 weeks post-treatment, 3 weeks post-treatment, and 4 weeks post-treatment (final day). Method of measurement: The percentage of wound healing will be determined by measuring the wound area at each visit and calculating the percentage reduction from the initial area. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHoda Mojiri Foroushani
Abadan University of Medical Sciences
Outcome results
None listed