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Comparison of the effect of sesame oil and 1% silver sulfadiazine ointment on the pain, healing and scarring of burn wounds

Comparison of the effect of sesame oil and 1% silver sulfadiazine ointment on the pain, healing and scarring of burn wounds

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180221038821N5
Enrollment
40
Registered
2023-02-05
Start date
2023-01-21
Completion date
Unknown
Last updated
2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn. Burn-out

Interventions

Intervention 1: Intervention group: Sesame oil group: For the sesame oil group, the burn wound dressing with sesame oil will first be washed with sodium chloride for washing and exposed to the open ai

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Informed consent to participate in the study Age 20-60 years First and second degree burns with an extent of 1-10% Burns due to contact with a heat source or liquids

Exclusion criteria

Exclusion criteria: Sesame oil allergy Confirmation of the need for hospitalization of the patient by the doctor Taking painkillers and NSAIDs orally or topically until the first visit to the treatment center Background diseases such as anemia, diabetes, cardiovascular diseases, malignancy and immune system defects Abnormal hemoglobin and total protein More than 6 hours passed from the time of the burn to the time of going to the medical center

Design outcomes

Primary

MeasureTime frame
Wound healing time. Timepoint: After confirming the healing of the wound by an emergency medicine specialist. Method of measurement: Questionnaire (Day).;The scar left by the wound. Timepoint: After confirming the healing of the wound by an emergency medicine specialist. Method of measurement: Beitz-Johnson Burn Wound Assessment Tool.

Secondary

MeasureTime frame
Intensity of pain. Timepoint: Before and after dressing in the first session. Method of measurement: Visual pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactIman Ghorbany Moghaddam

Gonabad University of Medical Sciences

imanghorbany135213@gmail.com+98 51 5722 0576

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026