Investigating effectiveness of smart biodegradable nanofiber dressing in the treatment of 2nd degree burn wounds
Phase 1
Recruiting
- Conditions
- Second degree burn.Burn and corrosion of head, face, and neck
- Registration Number
- IRCT20231122060138N1
- Lead Sponsor
- Zanjan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 16
Inclusion Criteria
Adult patient between 18 and 65 years old
Refer to the treatment center in less than 24 hours
Burn percentage ranges from 20-50%
Fill out the informed consent form
There should be at least 2 recorded records of the investigated variables.
Patients should stay in the hospital for at least three days
Exclusion Criteria
Having severe hypertension BP=160/90 mmHg
High cardiac troponin
pregnant women
Immune system defect
Anticoagulation problems, bleeding disorders, or heart disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ocal outcomes. Timepoint: At the beginning of the study (before the intervention) and 1, 3, 7, 14 and 28 days after applying the wound dressing. Method of measurement: Clinical observations and filling the checklist in 6 time points.;Systemic outcomes. Timepoint: At the beginning of the study (before the intervention) and 1, 3, 7, 14 and 28 days after applying the wound dressing. Method of measurement: Clinical observations and filling the checklist in 6 time points.
- Secondary Outcome Measures
Name Time Method Wound healing rate. Timepoint: At the beginning of the study (before the intervention) and 1, 3, 7,14, and 28 days after applying the wound dressing. Method of measurement: Based on examination done by evaluators.