Effect of Edible herbal oils on wound size
Phase 3
Recruiting
- Conditions
- Wound size.
- Registration Number
- IRCT20080901001174N11
- Lead Sponsor
- Rasht University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 112
Inclusion Criteria
Age of 15–65 years
Body mass index (BMI) of 18–30 kg/m2
Hospitalization for more than 24 hours
Admittion within 24 - 48 h post-burn
Willingness to participate
Able to feed through the mouth
Exclusion Criteria
Infected burn wounds
Cases of chronic and underlying diseases
Allergy to Flaxseed oil And Olive oil
The history of taking omega-3 and omega-6 in the previous week or month
pregnant and lactating women
Smoking
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wound size. Timepoint: Before intervention and 2, 9, 15, and 22 days after the intervention. Method of measurement: Getting photo from burn injury and measure the length and width of the wound to measure the area of the wound; Canon's camera model and a standard ruler will be used for this purpose. The area of the wound is measured by the AutoCAD software. Changing the area and the appearance of the wound will be considered as wound healing. When the wound appearance become pink and transparent with the non-secreting epithelium the wound will be considered as healed wound.
- Secondary Outcome Measures
Name Time Method Hs-CRP. Timepoint: At the beginning and at the end of the study. Method of measurement: Blood test.;Ferritin. Timepoint: At the beginning and at the end of the study. Method of measurement: Blood test.;Albumin. Timepoint: At the beginning and at the end of the study. Method of measurement: Blood test.