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The effect of silver sulfadiazine cream containing epidermal growth factor on diabetic foot ulcers.

Efficacy of Silversulfadiazine topical cream containing Epidermal growth factor (Bornamin) on the healing of Diabetic foot ulcer

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241027063508N1
Enrollment
50
Registered
2024-12-03
Start date
2024-12-05
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

diabetic foot ulcer. Type 2 diabetes mellitus with circulatory complications

Interventions

Intervention 1: Intervention Group: For this group, the standard treatment includes debridement and regular dressing along with 1 percent silver sulfadiazine cream combined with 0.001 percent epiderma

Sponsors

Borna Biopharma
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The age should be 18 years or older and less than 60 years. The patient should have a diabetic foot ulcer classified as grade 1 to 2 according to Wagner classification, with a maximum diameter of 5 centimeters The patient must not have severe vascular diseases, a history of any cancer or tumors, a history of any type of allergy to recombinant growth factors, a history of liver or kidney disease, as well as pregnancy and breastfeeding The patient must have the approval of a specialist physician to participate in the study.

Exclusion criteria

Exclusion criteria: The patient should not have underlying conditions that interfere with wound healing, such as severe vascular diseases, any form of cancer or tumors, and liver or kidney disease during the study. Observation of any type of allergy to the creams used is required Pregnancy during the study period is not allowed.

Design outcomes

Primary

MeasureTime frame
Diabetic foot ulcer healing speed. Timepoint: The size of the wounds and their characteristics at the beginning of the study and at each follow-up (weeks 1, 2, 3, 5, and 8 after enrollment) will be recorded by the physician. Method of measurement: In this study, wound healing is evaluated by measuring its area using ImageJ software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mehdi Tabaie

Tehran University of Medical Sciences

smtabaie@yahoo.com+98 21 6646 4862

Outcome results

None listed

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