Actively Recruiting

Phase Not Applicable
Age: 30Years - 59Years
All Genders
Healthy Volunteers
ID07467954

A Comparative Split-Face Study of Long-Pulsed 1064-nm Nd:YAG and Fractional CO2 Laser for Skin Rejuvenation Based on Dermal Thickness, Skin Elasticity, Wrinkle Assessment, and Global Aesthetic Improvement Scale Scores

Led by Universitas Padjadjaran · Updated on 2026-03-12

15

Participants Needed

1

Research Sites

5 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Skin rejuvenation aims to improve the signs of skin aging, which involve changes in the skin's layers including reduced collagen leading to thinner skin, laxity, and wrinkles. This trial evaluates and compares two types of laser therapies, fractional CO₂ laser and long-pulsed 1064-nm Nd:YAG laser, both used to stimulate collagen production and improve skin condition. The goal is to assess their effects on dermal thickness, skin elasticity, wrinkles, and overall aesthetic improvement in adults aged 30 to 59 with moderate skin aging.

CONDITIONS

Brief Title

Comparative Effectiveness of Long-Pulsed 1064-nm Nd:YAG and Fractional CO₂ Laser in Skin Rejuvenation

Who Can Participate

Age: 30Years - 59Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female patients with skin aging classified as Glogau scale II-III
  • Age between 30 and 59 years
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • Active smokers
  • Individuals with high levels of sun exposure
  • History of facial laser therapy, microdermabrasion, chemical peeling, botulinum toxin injection, microneedling, or skin booster injections within the past six months
  • Use of oral isotretinoin within the past six months
  • Use of topical retinoids or their derivatives, topical vitamin C, or other collagen-stimulating and skin-rejuvenating agents within the past two weeks
  • Use of oral vitamin C, collagen-stimulating supplements, antioxidants, or hormone therapy with skin-rejuvenating effects within the past one month
  • Presence of active facial skin inflammation
  • History of keloid formation
  • History of allergy to topical lidocaine anesthesia

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 3 months

Participants receive split-face laser treatments: fractional CO₂ laser on one randomized side of the face and long-pulsed 1064-nm Nd:YAG laser on the other side. Treatments are performed three times at one-month intervals to improve skin rejuvenation.

3 treatment visits at one-month intervals

Trial Site Locations

Total: 1 location

1

Hasan Sadikin General Hospital

Bandung, West Java, Indonesia, 40161

Actively Recruiting

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Research Team

A

Ahmad R Ganiem, M.D., Ph.D

K

Kartika Ruchiatan, M.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Frequently Asked Questions

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