Therapeutic effect of dressing containing silver on skin blister
Phase 3
Recruiting
- Conditions
- blister due to bone fracture.
- Registration Number
- IRCT20221207056744N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
all patients with blister due to bone fracture
aged between 18-65 years old
Consent to participate in the study
Exclusion Criteria
Sensitivity to silver
Amputation indication
patients who did not agree to participate in the study
those who did not participate in the study until the end and did not come for follow-up sessions
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wound area. Timepoint: Measurement of wound area at the beginning of the study (before the intervention), day 7 and day 14. Method of measurement: Taking a photo of the wound at a distance of 15 cm and perpendicular to the wound and analyzing it using the mosaic software.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: Measurements on day 0, 7 and 14. Method of measurement: VAS score questioner.;Duration of visit. Timepoint: Measurements on day 0, 7 and 14. Method of measurement: The length of time that the wound specialist visits the patient to change the dressing.;Number of dressings. Timepoint: From day 0 to day 14. Method of measurement: Counting the number of dressings by a wound expert.;Net cost of dressing. Timepoint: From day 0 to day 14. Method of measurement: The price of the total number of dressings used in the entire 14 days of the study.