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the efficacy of topical erythropoietin treatment on healing of second degree burned cutaneous burned wounds

Phase 3
Conditions
Burn.
Other disorders of skin and subcutaneous tissue in diseases classified elsewhere
Registration Number
IRCT20190810044500N23
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
48
Inclusion Criteria

Presenting to the burn center in the first 24 hours after the burn
Having grade II burns, superficial and deep, that involve less than 10% of the body's surface area
No comorbidity that delays the repair process (such as diabetes, chronic kidney disease, malignancy, and chronic use of corticosteroids)
Absence of respiratory burns as well as chemicals or electric burn
No burns on the face and perineum and hand

Exclusion Criteria

Concurrent infection during the study
Lack of response to treatment
The need for skin graft surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mean time of wound healing. Timepoint: The wound healing process is measured during the study period on days 1, 3, 7, 10, 14, and 21 after starting to use Erythropoietin cream on the wound area. Method of measurement: Clinical examination.;The rate of pigmentation. Timepoint: The rate of pigmentation is measured during the study period on days 1, 3, 7, 10, 14, and 21 after starting to use Erythropoietin cream in the wound area. Method of measurement: Clinical examination.;The rate of pain. Timepoint: The rate of pain is measured during the study period on days 1, 3, 7, 10, 14, and 21 after starting to use Erythropoietin cream in the wound area. Method of measurement: Clinical examination.;The rate of pruritus. Timepoint: The rate of pruritus is measured during the study period on days 1, 3, 7, 10, 14, and 21 after starting to use Erythropoietin cream in the wound area. Method of measurement: Clinical examination.
Secondary Outcome Measures
NameTimeMethod
Complications observed. Timepoint: End of the study. Method of measurement: Based on the doctor's observation and the person's statements.
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