Condition 1: burn wounds. Condition 2: burn wounds. Condition 3: burn wounds. Condition 4: burn wounds. Burn of unspecified degree of shoulder and upper limb, except wrist and hand Burn of unspecified degree of wrist and hand Burn of unspecified degree of unspecified site of lower limb, except ankle and foot Burn of unspecified degree of ankle and foot
Conditions
Interventions
Intervention 1: Intervention group: They will receive Plantago major cream and it will be applied twice a day on the surface of the wound. Intervention 2: Control group: Silver sulfadiazine cream 2 t
Sponsors
Fasa University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age 18 to 60 years Not having any underlying disease such as diabetes, seizures, nervous and mental disorders Not using corticosteroids and immunosuppressive drugs Insensitivity to medicinal plants Absence of pregnancy and breastfeeding No underlying skin disease Having 2nd degree thermal burns Burn percentage between 5 and 25% A maximum of 48 hours have passed since the burn Burns in the upper and lower limbs
Exclusion criteria
Exclusion criteria: Drug sensitivity History of mental illnesses Pregnancy and breastfeeding History of allergy to medicinal plants Chemical and electrical burns Burns other than upper and lower limbs Occurrence of skin complications during the treatment period The patient's lack of tolerance and his lack of satisfaction with the decision to continue the treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound size, redness, inflammation, edema. Timepoint: Before starting the study, days 5, 9, 13, 17, the end of the study. Method of measurement: The size of the wound with a ruler. Inflammation, redness and edema based on the standard wound questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Recovery time? wound infection. Timepoint: The healing time is measured according to the complete healing of the wound and the creation of new tissue. Infection in the days before the study and day 3, 7, 10. Method of measurement: Recovery time: observation of granulation tissue and new epithelium. The negative response to the infection was death. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahsa Rostami
Fasa University of Medical Sciences
Outcome results
None listed