Skip to content

Clinical study on the efficacy and safety of 1550nm and 1927nm dual-wavelength laser in the treatment of facial and neck photoaging and postoperative combined B5 repair application

Clinical study on the efficacy and safety of 1550nm and 1927nm dual-wavelength laser in the treatment of facial and neck photoaging and postoperative combined B5 repair application

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083929
Enrollment
Unknown
Registered
2024-05-08
Start date
2024-05-10
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

photoaging

Interventions

Observation group:Dual wavelength laser therapy +B5 repair dressing patch
Observation group :Dual wavelength laser therapy + control dressing patch

Sponsors

The First Affiliated Hospital, the Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age 30-75 years old, male or female; (2) Global Scores for Photoaging (GSP) 1-3 scores; (3) Fitzpatrick skin type was ? ~ ?; (4) Subjects agree to participate in this study and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Pregnant or planning pregnancy, breastfeeding women; (2) Scar constitution; (3) Have received intense light, chemical stripping, laser skin rejuvenation and other cosmetic treatments within 6 months; (4) Injections such as botox type A and filler therapy have been performed within 6 months; (5) Combined facial and neck infectious diseases are not suitable for laser treatment; (6) With active psoriasis, vitiligo and other easy to appear homotypic reaction; (7) Complicated with serious heart, lung, liver, renal insufficiency and other system diseases; (8) There is abnormal coagulation function and is receiving anticoagulant drug treatment; (9) There is a mental or serious mental illness; (10) Subjects who are not suitable to participate in this study, such as those who are unable to cooperate with the study interview and other researchers.

Design outcomes

Primary

MeasureTime frame
Using VISIA skin detector to measure changes in facial skin values before and after treatment;Using a CK system to measure changes in facial parameters before and after treatment;Using a 3D system to measure changes in facial parameters before and after treatment;

Secondary

MeasureTime frame
Subject satisfaction rating;Pain score;

Countries

China

Contacts

Public ContactGao Lin

The First Affiliated Hospital of the Air Force Medical University

gaolin@fmmu.edu.cn+86 187 2986 0707

Outcome results

None listed

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