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Skin RejuvenationNCT07467954

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

A study testing Fractional CO₂ laser and Long-pulsed 1064-nm Nd:YAG laser in people with Skin Rejuvenation and Laser, run by Universitas Padjadjaran at 1 site in Indonesia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Skin rejuvenation is an effort to improve skin condition from the signs of skin aging. Skin aging is a complex biological process influenced by intrinsic and extrinsic factors, leading to changes in the epidermis and dermis, including decreased collagen characterized by dermal thinning, as well as alterations in skin… Read more about this study

Who is it for?
Ages 30 to 59 yearsHealthy volunteers can take part
Conditions the study is for
Skin Rejuvenation, Laser
What is being tested?
Fractional CO₂ laser and Long-pulsed 1064-nm Nd:YAG laser
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
1 siteIndonesia
Study dates
14 Oct 2025to 16 Apr 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 59 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male and female patients with skin aging classified as Glogau scale II-III
  • Age 30-59 years.

Who cannot join

  • 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.
Show all 10Show fewer
  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

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

+62 878 2288 3773

rizalbdg@gmail.com

Kartika Ruchiatan, M.D. contact

+62 811 247932

kartika.ruchiatan@unpad.ac.id

Indonesia1 site, 1 recruiting
  • Hasan Sadikin General Hospital

    Bandung, West Java, 40161

    Recruiting

Other trials in Indonesia

About this study

Official title: 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

Skin rejuvenation is an effort to improve skin condition from the signs of skin aging. Skin aging is a complex biological process influenced by intrinsic and extrinsic factors, leading to changes in the epidermis and dermis, including decreased collagen characterized by dermal thinning, as well as alterations in skin appearance such as laxity and wrinkles. Laser therapy is one of the treatment modalities for skin rejuvenation, aiming to induce neocollagenesis and collagen remodeling, resulting in dermal thickening and improvement in skin appearance. Fractional CO₂ laser is an ablative laser considered the gold standard therapy for skin rejuvenation, whereas Long Pulsed (LP) Nd:YAG 1064 nm is a nonablative laser that is also used for skin rejuvenation. To date, there have been no studies evaluating the comparative effectiveness between fractional CO₂ laser and LP Nd:YAG 1064 nm for skin rejuvenation. Therefore, research comparing the effectiveness of fractional CO₂ laser and LP Nd:YAG 1064 nm for skin rejuvenation is needed, assessed based on dermal thickness, skin elasticity, wrinkles, and Global Aesthetic Improvement Scale scores.

Being tested
Fractional CO₂ laser, Long-pulsed 1064-nm Nd:YAG laser

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Fractional CO₂ laserProcedure or surgery

    Fractional CO₂ laser was applied to one randomized side of the face in a split-face design for skin rejuvenation. Treatments were performed three times at one-month intervals. The laser delivers fractional ablative microthermal zones to stimulate dermal remodeling and collagen production. Treatment parameters were adjusted according to skin type and clinical indication.

  • Long-pulsed 1064-nm Nd:YAG laserProcedure or surgery

    Long-pulsed 1064-nm Nd:YAG laser was applied to the contralateral randomized side of the face in a split-face design for skin rejuvenation. Treatments were performed three times at one-month intervals. The laser delivers non-ablative dermal heating to stimulate collagen remodeling and improve skin texture and elasticity.

Study groups in NCT07467954
Study groupRoleWhat they receive
Arm 1ExperimentalIn this split-face study, each participant received fractional CO₂ laser treatment on one side of the face. The treated side was randomly assigned. The procedure was performed three times at one-month intervals.
Receives: Procedure: Fractional CO₂ laser
Arm 2Active comparatorIn the same participants, the contralateral side of the face received long-pulsed 1064-nm Nd:YAG laser treatment. The side allocation was randomized. The procedure was performed three times at one-month intervals.
Receives: Procedure: Long-pulsed 1064-nm Nd:YAG laser

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Dermal Thickness

    Dermal thickness was assessed based on the two-dimensional area of the hyperechoic band that appears brighter than the epidermis on ultrasonography assessment.

    Measured: From enrollment to the end of treatment at 20 weeks

  2. Skin Elasticity

    Skin elasticity was defined as the ability of the skin to return to its original shape after deformation caused by mechanical traction. It was measured using a skin elasticity meter, and the R (recovery) value was assessed at 8 evaluation points on the face.

    Measured: From enrollment to the end of treatment at 20 weeks

  3. Wrinkles

    Lines or folds formed on the skin surface as a result of mechanical stress, skin dehydration, or repetitive muscular activity, and were evaluated using a facial skin analyzer

    Measured: From enrollment to the end of treatment at 20 weeks

  4. Global Aesthetic Improvement Scale Scores

    A 5-point rating scale (1-5) used to measure the degree of aesthetic improvement in patients following a procedure.

    Measured: From enrollment to the end of treatment at 20 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Mar 2026
  2. Study start14 Oct 2025
  3. Primary completion10 Mar 2026 (estimated)
  4. Study completion16 Apr 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
15 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07467954
Sponsor's protocol ID
DV-202603.01
Status last verified
Mar 2026
First submitted
8 Mar 2026
Last updated
12 Mar 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Fractional CO₂ laser and Long-pulsed 1064-nm Nd:YAG laser in people with Skin Rejuvenation and Laser, run by Universitas Padjadjaran at 1 site in Indonesia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 12 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Indonesia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Ahmad R Ganiem, M.D., Ph.D (+62 878 2288 3773, rizalbdg@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Dermal Thickness (time frame: From enrollment to the end of treatment at 20 weeks). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Mar 2026.

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