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Sesame oil and silver sulfadiazine in second degree burn

Comparing the effect of sesame oil and topical silver sulfadiazine 1% on improving the extent of burn and epithelialization of patients with second degree burn

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201188769N1
Enrollment
60
Registered
2012-09-19
Start date
2012-10-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Burn. Burn of second degree, body region unspecified

Interventions

Intervention 1: For the patients in control group topical Silver sulfadiazine 1% ointment (Made by Sina Daroo company of Iran, with trade name of Flamexin) is used once a day. The dosage is determ
Treatment - Drugs
Treatment - Other
For the patients in control group topical Silver sulfadiazine 1% ointment (Made by Sina Daroo company of Iran, with trade name of Flamexin) is used once a day. The dosage is determined based on t
For the patients in case group pure topical sesame oil (Made by Merk company of Germany) is used once a day. The dosage is determined based on the extent of the lesion

Sponsors

Vice chancellor for Education, Research and Technology of Qom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients hospitalized with second degree burns in the burn center of Nekoi Hospital of Qom Exclusion criteria: Age less than 2 years, comorbidity with diseases, inhalation burns, third degree burns, burns over 25% of body surface

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The extent of burn. Timepoint: Before the intervention and every three days until epithelialization. Method of measurement: Ruler and extent based on square centimeters.

Secondary

MeasureTime frame
The need for antibiotic. Timepoint: Every day until discharge. Method of measurement: Number of doses.;The need for analgesic drugs. Timepoint: Every day until discharge. Method of measurement: Number of doses.;The extent of residual scar. Timepoint: Weekly after the intervention until one month after full recovery. Method of measurement: Ruler and extent based on square centimeters.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Jalal Eshagh Hosseini, MD.

Qom University of Medical Sciences

j.hosseini@muq.ac.ir+98 25171181

Outcome results

None listed

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