Health Condition 1: L910- Hypertrophic scar
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients undergoing the following surgeries - breast augmentation, double incision mastectomy, reduction mammoplasty and mastopexy 2) 3 weeks post-op or after suture removal 3) Willingness to adhere to follow-up
Exclusion criteria
Exclusion criteria: 1) Prior scar treatment (laser, PRP, intralesional steroid, microneedling) 2) Keloid/hypertrophic scar history 3) Uncontrolled diabetes or hypertension 4) Refusal of consent or inability to adhere to follow-up
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare overall scar quality (Vancouver Scar Scale, VSS) at 6 months between the three groups (Erbium:Glass laser (NAFL) + standard care, CO2 laser (FAL) + standard care, Standard Care only (Silicone gel/ sheet)Timepoint: 3 weeks, 3 months and 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in Scar Thickness and Echogenicity using High Frequency Ultrasound (HFUS) Patient satisfaction with scar quality (Likert scale) Incidence of adverse events (post-treatment hyperpigmentation [PTH], delayed healing, infection, pain)Timepoint: 3 weeks, 3 months and 6 months | — |
Countries
India
Contacts
ALL INDIA INSTITUTE OF MEDICAL SCIENCES NEW DELHI