ClinicalTrials.gg
RecruitingNCT07472192PDRN CO2 LASERUpdated Mar 16, 2026

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

A Phase 2 interventional study of Polydeoxyribonucleotide and Fractional CO2 laser assisted PDT in Facial Scarring, sponsored by Misr University for Science and Technology. Recruiting at 1 site in Egypt. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-03-16.

Sponsored by Misr University for Science and Technology · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2026, 4 months ago, but the record still lists the study as recruiting.
  • Started Mar 2026; still recruiting 8 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Facial Scarring
03

In context

Lead sponsor

Misr University for Science and Technology is the lead sponsor of 38 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 and engage in all aspects of the study.

Exclusion criteria

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 .
    • Anticoagulants.
  • Uncontrolled medical diseases (e.g., unstable diabetes, cardiac conditions).
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
36 participants (estimated)

Study arms

  • Active comparator
    Fractional Carbon Dioxide Laser Combined with Polydeoxyribonucleotide (PDRN)

    includes patients who will be enrolled for PDRN injection into the surgical scar

    Drug: Polydeoxyribonucleotide · Device: Fractional CO2 laser assisted PDT

  • Placebo comparator
    Fractional CO₂ laser therapy with placebo saline injection

    includes patients who will be enrolled for placebo saline injection into the surgical scar

    Device: Fractional CO2 laser assisted PDT

Interventions

  • intralesional PDRN injections

  • DeviceFractional CO2 laser assisted PDT

    Fractional carbon dioxide (CO₂) laser therapy for facial scars

    Also known as: co2 laser

06

What researchers measure

Primary outcomes

  1. Vancouver Scar Scale

    The study used the standard Vancouver Scar Scale, which evaluates four characteristics of scars: Total Score Range: 0 (normal skin) to 13 (severe hypertrophic scar)

    Time frame: 4 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

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. PubMed 29574803 ↗

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2026 (actual). Primary completion is estimated for Jul 2026, 4 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 11, 2026
First posted
Mar 16, 2026
StartActual
Mar 1, 2026
Primary completionEst.
Jul 1, 2026
CompletionEst.
Jul 1, 2026
Last update
Mar 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07472192
Lead sponsor
Misr University for Science and Technology
Responsible party
Omnia Tarek Hosni (Demonstrator in Oral & Maxillofacial Surgery Department, MUST, Misr University for Science and Technology) — Principal investigator
First posted
Mar 16, 2026
Start date
Mar 1, 2026
Primary completion
Jul 1, 2026 (estimated)
Completion
Jul 1, 2026 (estimated)
Last update
Mar 16, 2026

Study contacts

Omnia Tarek Hosni
Contact
200048686@must.edu.eg
01117196173 ext. 002

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Polydeoxyribonucleotides

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