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Comparative Study of a 1064-nm Fractional Picosecond Laser Versus IPL in Facial Rejuvenation

Fudan University logo

Fudan University

Status

Completed

Conditions

Skin Rejuvenation
Skin Aging
Photoaging

Treatments

Device: Intense Pulsed Light Therapy (M22 IPL System)
Device: 1064-nm Fractional Picosecond Laser (PicoWay)

Study type

Interventional

Funder types

Other

Identifiers

NCT07122310
KY2022-824

Details and patient eligibility

About

This is a single-center, prospective, randomized controlled trial conducted at Huashan Hospital, Fudan University. The purpose of this study is to compare the effectiveness and safety of two non-invasive treatment options-1064-nm fractional picosecond laser and intense pulsed light (IPL)-for facial rejuvenation. A total of 38 participants seeking cosmetic improvement were randomly assigned to receive three sessions of either picosecond laser or IPL treatment at 4-6 week intervals.

Each participant was monitored throughout the treatment period and at one month after the final session. The study assessed improvements in skin texture, pigmentation, and wrinkles, as well as treatment-related side effects. All participants provided informed consent and received standardized post-treatment care instructions, including moisturization and sun protection. The results of this study may help guide non-surgical treatment options for skin aging.

Enrollment

38 patients

Sex

Female

Ages

30 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

(1)Individuals aged 30-60 years with a GSP score of 1-4;(2)Fitzpatrick skin phototypes III-IV;(3)Written informed consent obtained.

Exclusion criteria

(1)Pregnant or lactating women;(2)Patients with severe systemic diseases;(3)Individuals with coagulation dysfunction;(4)Patients with mental disorders;(5)Photosensitive individuals;(6)Individuals with infections at the treatment site;(7)Individuals who have used photosensitive drugs within 4 weeks;(8)Individuals who have received other cosmetic treatments such as laser, intense pulsed light (IPL), radiofrequency, chemical peels (e.g., glycolic acid), fillers, etc., within 6 months;(9)Individuals with a personal or family history of keloids;(10)Individuals with a personal or family history of cutaneous squamous cell carcinoma or melanoma;(11)Individuals with a personal or family history of vitiligo;(12)Individuals with a history of intense sun exposure or ultraviolet (UV) radiation within 1 month.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

38 participants in 2 patient groups

Picosecond Laser Group
Experimental group
Treatment:
Device: 1064-nm Fractional Picosecond Laser (PicoWay)
Intense Pulsed Light (IPL) Group
Experimental group
Treatment:
Device: Intense Pulsed Light Therapy (M22 IPL System)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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