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A Study on CO2 Laser-Assisted Skin Openings (Macro versus Micro) for Better Drug Entry and Treatment Result

A Comparative analysis of co2 laser assisted macro-coring versus micro-coring for enhanced drug delivery of triamcinolone acetonide - assessment of clinical outcomes and therapeutic safety. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/098040
Enrollment
10
Registered
2025-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health Condition 1: L910- Hypertrophic scar

Interventions

Intervention1: CO2 laser assisted macro coring: CO2 laser assisted macro coring of keloid tissue using a 1 to 2 mm probe spaced 1 mm apart, followed by intralesional triamcinolone acetonide injection

Sponsors

CUTIS Academy of Cutaneous Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of either gender, above the age of 15to 70 years (guardians consent). 2.Patients having single or multiple clinically diagnosed keloids. 3.Patients having keloids over any region of the body. 4.Duration of lesions more than 6 months. 5.Patients not on any surgical treatment for the past 3 months. 6.Patients consenting for study and willing for follow up.

Exclusion criteria

Exclusion criteria: 1. Patients with infected keloids or coexisting inflammatory systemic skin diseases 2. Unrealistic expectations or psychiatric illnesses 3. Pre existing bleeding disorders 4. Lactating/pregnant patients

Design outcomes

Primary

MeasureTime frame
Change in keloid volume from baseline to 12 weeks, measured using 3D profilometry-derived volume metrics via Antera 3D Imaging System (Miravex, Ireland).Timepoint: After Week 12

Secondary

MeasureTime frame
Changes in keloid surface texture, vascularity, and pigmentation will be objectively assessed using Antera 3D imaging. Clinician assessments will include the Vancouver Scar Scale and POSAS Observer Scale, while patient feedback will be recorded using the POSAS Patient Scale, VAS for pain and itch, and a satisfaction Likert scale. Recurrence and time to recurrence will also be monitored through Antera 3D parameters during follow-up.Timepoint: After Week 12

Countries

India

Contacts

Public ContactDr Madura C

CUTIS Academy of Cutaneous Sciences

maduradr@gmail.com9632741998

Outcome results

None listed

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