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EFFICACY AND SAFETY OF 1064-NM FRACTIONAL PICOSECOND LASER COMBINED WITH MICRONEEDLE RADIOFREQUENCY VERSUS PICOSECOND LASER ALONE FOR THE TREATMENT OF ATROPHIC ACNE SCARS: A SPLIT-FACE RANDOMIZED CONTROLLED TRIAL

EFFICACY AND SAFETY OF 1064-NM FRACTIONAL PICOSECOND LASER COMBINED WITH MICRONEEDLE RADIOFREQUENCY VERSUS PICOSECOND LASER ALONE FOR THE TREATMENT OF ATROPHIC ACNE SCARS: A SPLIT-FACE RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260511013
Enrollment
22
Registered
2026-05-11
Start date
2026-05-08
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Atrophic acne scars Acne scars Atrophic acne scars Picosecond laser Fractional laser therapy Microneedling Radiofrequency therapy Randomized controlled trial

Interventions

1064 nm fractional picosecond laser treatment is performed on one side of the face for the treatment of atrophic acne scars. Participants receive 3 treatment sessions at 1 month intervals.,1064 nm fra
Experimental Device,Experimental Device
1064 nm fractional picosecond laser alone,1064 nm fractional picosecond laser combined with microneedle radiofrequency

Sponsors

Dhurakij Pundit University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Male or female adults aged 20 to 60 years 2. Moderate to severe atrophic acne scars with Goodman and Baron scale grade 3 or 4 3. Fitzpatrick skin types III to IV 4. Willing to participate in the study and able to provide written informed consent

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding women 2. Allergy to local anesthetics 3. Facial acne scar laser treatment within the past 6 months 4. Facial aesthetic procedures within the past 3 months 5. Active facial dermatitis, open wounds, or skin infection on the face 6. Immunodeficiency, including HIV infection 7. Oral retinoid use within the past 3 months 8. History of keloid or abnormal scar formation in the treatment area 9. Systemic diseases such as diabetes, thyroid disease, or cancer 10. Smoking 11. Psychiatric disorders 12. Any condition considered unsafe by the investigator

Design outcomes

Primary

MeasureTime frame
Depressed scar volume Baseline, Week 12, Week 20 Antera 3D,Texture Baseline, Week 12, Week 20 Antera3D

Secondary

MeasureTime frame
Erythema index Baseline, Week 12, Week 20 Mexameter,Melanin index Baseline, Week 12, Week 20 Mexameter,Quartile grading scale Baseline, Week 12, Week 20 by two dermatologists,Pain score 1st, 2nd, 3rd treatment Visual analog scale,Participant satisfaction Week 12, Week 20 Global Aesthetic Improvement Scale,Safety 1st, 2nd, 3rd treatment Adverse events

Countries

Thailand

Contacts

Public ContactWanvisa Silpaiboonpanich

Dhurakij Pundit University

sil.wanvisa@gmail.com029547300

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026