Burn patients. Burn and corrosion of head, face, and neck
Conditions
Interventions
Intervention 1: Intervention group: The topical gel containing insulin and silver nanoparticles is used for two weeks and this dressing in the treatment of burn wounds accelerates wound healing, reduc
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
2 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients between the ages of 2 and 60 are eligible to participate. Patients with second-degree burns diagnosed by the relevant physician Patients with burns that are less than or equal to 20% Patient with second-degree burns in upper and lower limbs and anterior trunk The wound is examined by a plastic and burn surgeon for necrosis and the depth of the burn. If the burned area is not a candidate for early surgery and can be healed without surgery and with minimal complications, the patient will be eligible to the study
Exclusion criteria
Exclusion criteria: Delayed visit and the presence of obvious wound infection at the first visit by an infectious disease specialist Patients who are receiving chemotherapy Patients taking corticosteroids or cytotoxic medicines Pregnancy Cancer, cytotoxic drugs, immunosuppressants, and the presence of chronic diseases other than diabetes that affect wound healing, such as severe vascular disease, lupus, rheumatoid arthritis, and renal failure Smoking The presence of an underlying disease leads to a defective immune system Diabetic patients Taking drugs that lead to a defective immune system. Burns in the back of the trunk, face, head and perineum
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of complete wound healing. Timepoint: Every 48 hours. Method of measurement: Based on the clinical observations of an infectious disease specialist and plastic and burn surgeon. | — |
Secondary
| Measure | Time frame |
|---|---|
| Wound condition (presence or absence of granulation tissue, bleeding, pain, infection, and other wound complications or healing factors). Timepoint: Every 48 hours for 2 weeks. Method of measurement: Based on the scores of the variables and presence or absence (yes / no) and based on clinical observations of an infectious disease specialist and subspecialty of plastic surgery and burns. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Omid Yazarlou
Mashhad University of Medical Sciences
Outcome results
None listed