Actively Recruiting
Comparative Study for Facial Scar Remodeling Using Fractional Carbon Dioxide Laser Combined With PDRN Versus Fractional CO₂ Laser
Led by Misr University for Science and Technology · Updated on 2026-03-16
36
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Facial scars are frequently deemed unpleasant and can profoundly impact a patient's psychological health. This study compares the effectiveness, safety, and capacity to speed up scar healing in the maxillofacial region between fractional carbon dioxide (CO₂) laser therapy alone and polydeoxyribonucleotide (PDRN) combined with CO₂ laser therapy.
CONDITIONS
Official Title
Comparative Study for Facial Scar Remodeling Using Fractional Carbon Dioxide Laser Combined With PDRN Versus Fractional CO₂ Laser
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be between 18 and 50 years of age
- Facial wounds or surgical scars must be recent, about 1 to 6 months old
- Willingness to provide informed consent and participate fully in the study
You will not qualify if you...
- Pregnant or breastfeeding at the time of study
- Known allergy to polydeoxyribonucleotide (PDRN)
- Use of medications that affect wound healing or inflammation such as isotretinoin, anticancer drugs, high-dose corticosteroids, or anticoagulants
- Uncontrolled medical diseases like unstable diabetes or heart conditions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Misr University for Science and Technology
Giza, Egypt
Actively Recruiting
Research Team
O
Omnia Tarek Hosni
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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