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Evaluation of the effectiveness of fractional CO2 laser and PRP in comparisonwith fractional CO2 laser in treatment of burn scar

Evaluation of the effectiveness , satisfaction and complication of fractional CO2 laser and PRP in comparisonwith fractional CO2 laser in treatment of burn scar

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200127046282N9
Enrollment
10
Registered
2022-03-28
Start date
2022-04-19
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

burn scar. Atrophic disorders of skin

Interventions

Intervention 1: Intervention group: Patients with fractional CO2 laser with PRP will receive three sessions one month apart. Intervention 2: Control group: Patients will receive fractional CO2 laser a

Sponsors

Skin and Stem Cell Research Center, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients with skin type 1-4 Patients with atrophic burn scars in more than one organ from 5 years ago to 3 months ago

Exclusion criteria

Exclusion criteria: Age under 18 years Patients who have received laser treatment in the last three months Patients with active colloidal scar or active skin lesion at the injection site Patients with coagulation and platelet disorders Patients with a history of anticoagulants Patients with a history of underlying disease such as diabetes and autoimmune connective tissue disease that affect wound healing Patients with active viral infections History of malignancy or receiving chemotherapy Pregnancy and lactation

Design outcomes

Primary

MeasureTime frame
Scar size. Timepoint: before and 2 month after the intervention. Method of measurement: visio face.

Secondary

MeasureTime frame
Side effects. Timepoint: One week after treatment. Method of measurement: Questionnaire and visit.;Patient Satisfaction. Timepoint: Two months after treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSona Zare

Tehran University of Medical Sciences

sonazarebio@gmail.com+98 21 2665 7438

Outcome results

None listed

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