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Recruiting NCT07472192

Comparative Study for Facial Scar Remodeling Using Fractional Carbon Dioxide Laser Combined With PDRN Versus Fractional CO₂ Laser

Phase II Interventional Facial Scarring

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Polydeoxyribonucleotide, Fractional CO2 laser assisted PDT.
Who it may be relevant to
Registry conditions: Facial Scarring. Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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

Overview

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.

Interventions

  • Drug Polydeoxyribonucleotide
    intralesional PDRN injections
  • Device Fractional CO2 laser assisted PDT
    Fractional carbon dioxide (CO₂) laser therapy for facial scars

Primary outcome measures

  • Vancouver Scar Scale [Time frame: 4 months]

Eligibility 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).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Misr University for Science and Technology — Giza

Publications

  • Kim JH, Jeong JJ, Lee YI, Lee WJ, Lee C, Chung WY, Nam KH, Lee JH. Preventive effect of polynucleotide on post-thyroidectomy scars: A randomized, double-blinded, controlled trial. Lasers Surg Med. 2018 Mar 25. doi: 10.1002/lsm.22812. Online ahead of print. PMID 29574803

Identifiers

NCT: NCT07472192 · 011

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗