Burn of second degree. Burn of second degree, body region unspecified
Conditions
Interventions
Intervention 1: Intervention group: The studied patients are dressed with pumpkin seed oil by the researcher once a day for a period of 14 days. The experimental group is treated with pumpkin seed oil
The first session before the start of treatment, the third day, the seventh day and the day of the clear start of epithelization, the day of recovery and the fourteenth day after the start of treatmen
Sponsors
Yasouj University of Medical Sciences
Eligibility
Sex/Gender
All
Age
2 Years to 7 Years
Inclusion criteria
Inclusion criteria: The cause of thermal burns Consent to participate in the study Age 2 to 7 years Second degree burn and below 20% and thermal type Burns in the hands and feet except the fingers Do not wash excessively with water and detergents Not having diseases that weaken the immune system The child's face is healthy and does not suffer from any congenital malformation, especially in the organs and face, and does not have trauma in the organs
Exclusion criteria
Exclusion criteria: Lack of parental consent Creating an active infection at the site of the lesion Use of topical immunosuppressants within four weeks before starting treatment Local infection Any vascular disease of the brain, cardiovascular Patients needing a skin graft for treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound healing score of Bates-Jensen Wound Assessment Tool. Timepoint: The first session before the start of treatment, the third day, the seventh day and the day of the clear start of epithelization, the day of repair and the fourteenth day after the start of treatment. Method of measurement: Bates-Jensen Wound Assessment Tool for healing of burn.;Pain severity. Timepoint: The first session before the start of treatment, the third day, the seventh day and the day of the clear start of epithelization, the day of repair and the fourteenth day after the start of treatment. Method of measurement: Face, Legs, Activity, Cry, Consolability scale (FLACC scale). | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain degeneration. Timepoint: The first session before the start of treatment, the third day, the seventh day and the day of the clear start of epithelization, the day of repair and the fourteenth day after the start of treatment. Method of measurement: Bates-Jensen Wound Assessment Tool. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohsen Salari
Yasouj University of Medical Sciences
Outcome results
None listed