Study of the efficacy of a topical burn ointment dressing versus traditional Vaseline gauze dressing in burn treatment
Not Applicable
- Conditions
- Burn.Burns and corrosions of external body surface, specified by siteT20-25
- Registration Number
- IRCT2013011312107N1
- Lead Sponsor
- Morvarid co.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Inclusion criterion: burn lesions of 1 and 2 degrees, based on clinical examination, occured not more than 6 hours before randomization.
Exclusion criteria: unwillingness to enter the study; being a candidate for inpatient treatment; need to antibiotics; suffering diabetes mellitus or renal failure; using immune suppressors and if she is pregnant.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: One hours after treatment. Method of measurement: Questionnaire.;Blister formation. Timepoint: The begining of the study, first prescription, second prescription. Method of measurement: Objective.;Burn lesion secretion. Timepoint: First, second and third prescriptions. Method of measurement: Objective.
- Secondary Outcome Measures
Name Time Method