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Comparative study of the effect of a mixture of cerium nitrate and silver sulfadiazine with silver sulfadiazineointment on the healing of deep second-degree burn wounds , Shiraz -Intervention - Randomized controlled clinical trial

Comparative study of the effect of a mixture of cerium nitrate and silver sulfadiazine with silver sulfadiazineointment on the healing of deep second-degree burn wounds i -Intervention - Randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180609040016N8
Enrollment
60
Registered
2026-05-25
Start date
2026-08-29
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Comparative study of the effect of a mixture of cerium nitrate and silver sulfadiazine with silver sulfadiazineointment on the healing of deep second-degree burn wounds in patients referred to Amir-Al-Monin Hospital, Shiraz -Intervention - Randomized controlled clinical trial.

Interventions

Intervention 1: Intervention group: Group A (intervention) will be applied a dressing containing a mixture of cerium nitrate and silver sulfadiazine. The dressing will be applied in such a way that th

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to No maximum

Inclusion criteria

Inclusion criteria: The inclusion criteria for the study included patients aged 18 to 60 years, patients who had burns due to contact with a heat source or liquids, no more than 1 day had passed since the burn, the extent of the burn in the area of ??interest was less than 5% and the burn was a second-degree burn, no intubation, and a body mass index greater than 18 and less than 25.

Exclusion criteria

Exclusion criteria: patients with skin diseases and skin allergies to herbal medicines, patients with underlying diseases such as anemia, diabetes, cardiovascular diseases, malignancy, immune system deficiency, chronic renal failure, liver failure, trauma, poisoning, and joint infections, , patients with pregnancy patients with allergies to any of the ointments used

Design outcomes

Primary

MeasureTime frame
Amount of pain. Timepoint: After washing the wound before and after dressing. Method of measurement: Inspection.

Secondary

MeasureTime frame
Recovery rate. Timepoint: Cultures will be sent from the patient's wound on days 3, 7, 10, 13, and 21. Method of measurement: Inspection.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbdolkhalegh Keshavarzi

Shiraz University of Medical Sciences

iliakeshavarzi@yahoo.com+98 71 3614 6100

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026