Evaluation of the effects of a topical spray containing effective herbal ingredients on burn wound
Phase 3
- Conditions
- Second and third- degree burns.Burns and corrosions of external body surface, specified by siteT20-T25
- Registration Number
- IRCT20240221061068N1
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Age group 10 to 70 years
Having first and second degree burns involving at least 1 cm2 of body area surface
Full consciousness so that she/he is able to understand the instructions and take care of herself (including not rubbing, touching and scratching the burn site)
Exclusion Criteria
Hypersensitivity to herbal spray formulation
having a history of asthma, COPD, hay fever, rhinitis and skin sensitivity
Having a skin lesion that prevents the evaluation of the burn wound.
?eceiving anti-inflammatory drugs(eg, glucocorticosteroids and NSAIDs)
Concurrent participation in another clinical trial to investigate an agent affecting burns
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Burn wound healing percentage. Timepoint: The wound area of all participant will be calculated every 24 hours during study. Method of measurement: To calculate the wounds areas, photographs will be taken of the wounds and the area of each wound will be calculated using ImageJ image analysis software.
- Secondary Outcome Measures
Name Time Method