2nd degree burn wounds. burn
Conditions
Interventions
Intervention 1: Control group: In the control group, 1% silversulfadiazine ointment will be placed directly on all the patients wounds by a plastic surgeon and bandaged. The wounds of all patients who
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
8 Years to No maximum
Inclusion criteria
Inclusion criteria: Age more than 8 years The interval between the start of treatment and the occurrence of burns should be less than 24 hours. Suffering from 2nd degree burns and the amount of superficial skin burns should be less than 20%. Being alert and having the ability to communicate verbally Patients whose body mass index is more than 18.5 and less than 30.
Exclusion criteria
Exclusion criteria: Patients with mental disorders Patients whose burns are caused by electricity, chemicals, inhalation or self-immolation. Patients who do not want to cooperate at the beginning of the intervention or during the intervention. Patients suffering from severe respiratory diseases or asthma and allergic diseases or showing allergic symptoms to the treatment. Patients with a history of metabolic diseases, coagulation disorders, immunodeficiency, vascular, diabetes, kidney failure Patients who are undergoing treatments that change the state of wound healing (such as corticosteroids, chemotherapy, radiotherapy) Women who are pregnant or breastfeeding. Patients with head and neck burns Infection of patients' wounds during research Patients who are active or inactive smokers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The extent of the wound. Timepoint: Before starting the intervention and then every 5 days until the wound heals. Method of measurement: ruler.;The time it takes for the wound to heal. Timepoint: Before starting the intervention and then every 5 days until the wound heals. Method of measurement: The clinical diagnosis of a plastic surgery doctor based on the reepithelialization of more than 95% of the wound surface. | — |
Secondary
| Measure | Time frame |
|---|---|
| Microbial culture from the wound surface. Timepoint: Before the intervention and the fifth day and 20th day. Method of measurement: Swab sampling from the wound bed and its culture in the laboratory.;Intensity of pain. Timepoint: before the start of the intervention and then on the fifth day, the tenth day and then with 10-day intervals until the wound heals. Method of measurement: VAS questionnaire --- HUSKISSON, Edward C. Measurement of pain. The lancet, 1974, 304.7889: 1127-1131.?.;Intensity of itching. Timepoint: before the start of the intervention and then on the fifth day, the tenth day and then with 10-day intervals until the wound heals. Method of measurement: Burns itch questionnaire --- VAN LOEY, N. E., et al. Validation of the burns itch questionnaire. Burns, 2016, 42.3: 526-534.?. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAmir Mohammad Zamani
Ahvaz University of Medical Sciences
Outcome results
None listed