Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 18 to 50

Facial scar remodeling with fractional CO2 laser plus PDRN versus CO2 laser alone

Official title: Comparative Study for Facial Scar Remodeling Using Fractional Carbon Dioxide Laser Combined With Polydeoxyribonucleotide (PDRN) Versus Fractional CO₂ Laser: A Randomized Controlled Clinical Study

Run by Misr University for Science and Technology · NCT07472192 · Data updated 2026-11-12

This test checks whether adding PDRN injections to fractional CO2 laser treatment helps adults (18–50) with recent facial surgical or cut scars (1–6 months old) heal faster and look better than laser alone.

Quick facts

PhasePhase 2
Study typeInterventional
Ages18 Years to 50 Years
SexAll
Enrollment36 (estimated)
SponsorMisr University for Science and Technology
Academic / other
Locations1 site (Giza)
StatusRecruiting
StartedMarch 1, 2026
Main results expectedJuly 1, 2026
Study endsJuly 1, 2026
Registry record updatedMarch 16, 2026
Trial IDNCT07472192 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–50 with recent (1–6 month) facial surgical or cut scars who can attend in-person visits and provide informed consent.

Probably not a fit

People who are pregnant or breastfeeding, allergic to PDRN, taking medications that affect wound healing, or with uncontrolled medical conditions are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This Phase 2 interventional study compares two approaches for remodeling maxillofacial scars: fractional CO2 laser alone versus fractional CO2 laser combined with polydeoxyribonucleotide (PDRN). Eligible adults receive one of the two treatment approaches and are followed for clinical signs of scar improvement, healing speed, and safety outcomes. The study excludes pregnant or breastfeeding people, anyone allergic to PDRN, and those on medications or with conditions that impair wound healing. Outcomes are measured by clinical assessments and safety monitoring during scheduled in-person visits at the study site.

Why it matters

Potential benefit: If successful, combining PDRN with fractional CO2 laser could speed healing and improve the appearance of recent facial scars compared with laser alone.

How similar studies have gone: Fractional CO2 laser is an established scar treatment and small studies suggest PDRN may aid wound healing, but evidence for the combined approach is still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age Limitations: Participants must be between 18 and 50 years of age.
* Recently cut wounds or surgical scars from about (1-6 months).
* Consent to Participate: Willingness to provide informed consent and engage in all aspects of the study.

Exclusion Criteria:

* Pregnancy or breastfeeding at the time of study.
* Known allergy to PDRN.
* Medication use that could affect wound healing or inflammation, such as:

  * Isotretinoin.
  * Anticancer drugs.
  * High-dose corticosteroids.
  * Anticoagulants.
* Uncontrolled medical diseases (e.g., unstable diabetes, cardiac conditions).

Where it's running

  • Misr University for Science and Technology
    Giza, Egypt
    Recruiting

Study contacts

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.