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The effect of fractional CO2 laser in combination with topical insulin in treatment of facial atrophic acne scars

The safety and efficacy of Fractional CO2 laser with topical insulin versus Fractional CO2 laser alone in facial atrophic post-acne scar: A randomized split-face study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086346
Enrollment
30
Registered
2025-05-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: L700- Acne vulgaris

Interventions

Intervention1: Fractional CO2 with Topical insulin: In each visit, the Fractional CO2 Laser (Fotona, SP Dynamics) with parameters Wavelength-10600nm, point energy- 8 mJ, 8W, residence time- 1ms, Inte

Sponsors

IMS AND SUM HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Atrophic post Acne scar of any grade Fitzpatrick skin type 3 to 6 No treatment (including surgical and laser therapy) within 12 weeks before being enrolled in the study.

Exclusion criteria

Exclusion criteria: Pregnancy and lactation Autoimmune disease, connective tissue disease History of Photosensitivity Use of immunosuppressive medications, active cancer, underlying illness (cardiac, neurological) History of skin cancers, and presence of premalignant or malignant cutaneous lesions over the face. History of keloidal tendency Patient on isotretinoin therapy Presence of hypertrophic scars History of diabetes mellitus

Design outcomes

Primary

MeasureTime frame
To Compare the efficacy of topical insulin with fractional CO2 laser versus fractional CO2 alone in the treatment of PAS.Timepoint: 0 week,4 weeks,8 weeks,12 weeks

Secondary

MeasureTime frame
To Assess the safety of topical insulin with fractional CO2 laser in the treatment of PAS. To Assess the effect of topical insulin with fractional CO2 laser therapy on the quality of life in PAS patients Timepoint: 0 week,4 weeks,8 weeks,12 weeks

Countries

India

Contacts

Public ContactBikash Ranjan Kar

IMS AND SUM HOSPITALS

bikashkar@soa.ac.in9937428181

Outcome results

None listed

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