second degree burn. Burn of second degree, body region unspecified
Conditions
Interventions
Intervention 1: Intervention group 1: Calendula, capsule of 500 mg orally, twice daily for fourteen days. Intervention 2: Control group: Starch,A capsule of 500 mg orally, twice daily for fourteen day
Placebo
Intervention group 1: Calendula, capsule of 500 mg orally, twice daily for fourteen days
Control group: Starch,A capsule of 500 mg orally, twice daily for fourteen days
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: Second degree burns; Burn percentage between 15 and 50% (based on Landau Browder chart); The samples should be between the ages of 18 and 55 years; Over 48 hours of burn injury; In the burn area, be hospitalized; Do not be fast; Participate in the study; Not pregnant; Do not breastfeed; Lack of underlying diseases such as diabetes, cancer, or infectious diseases; Do not abuse substance (alcohol, narcotics, and sedation). Exclusion criteria: Unwillingness to continue to study; Release of patient; Transfer to another department; Patient's death
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound healing. Timepoint: In the days of 1,7 and 15. Method of measurement: BATES-JENSEN WOUND ASSESSMENT TOOL. | — |
Secondary
| Measure | Time frame |
|---|---|
| Burn percentage. Timepoint: In the days of 1,7 and 15. Method of measurement: Landau Brothers Chart.;Burn depth. Timepoint: In the days of 1,7 and 15. Method of measurement: BATES-JENSEN WOUND ASSESSMENT TOOL. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSORAYA REZAEE
Arak University of Medical Sciences
Outcome results
None listed