Burn wound. Burns and corrosions
Conditions
Interventions
Intervention 1: Intervention group: In the study group, after washing the wound with normal saline, a relatively thick layer of Recove ointment to be used and dressing is doing with sterile gauze. Pre
Treatment - Drugs
Intervention group: In the study group, after washing the wound with normal saline, a relatively thick layer of Recove ointment to be used and dressing is doing with sterile gauze. Prescription of ora
Control group: Patients enrolled in the control group are treated according to routine care of emergency room, including washing with normal saline, and dressing with topical Nitrofurazon cream 0.2% a
Sponsors
Tosan darou
Eligibility
Sex/Gender
All
Age
12 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: patients between 12-70 years old with burn injury including grade 1 and 2 that have burned during 6 hours before admission. Exclusion criteria: Dissatisfaction to enter the study; more than 10% TBSA burn; Need to be hospitalized; Burn wounds in head, face or genitalia; Electrical and Chemical Burns; Need to intravenous analgesic; Immunodeficiency; Diabetics; using Corticosteroid; uncontrolled hypertension; Withdrawing from the study; burn wound infection proved through clinical examination; Technical or human error in the process of treatment.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: First hour after dressing. Method of measurement: Numerical Scale.;Blister. Timepoint: first day. Method of measurement: Observation.;Microbial control. Timepoint: The 4th day. Method of measurement: Wound cultures in EMB& Blood Agar.;Wound healing. Timepoint: First day, 4th day, 10th day. Method of measurement: Photo and observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactParviz Namazi
Iran University of Medical Science
Outcome results
None listed