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Negative-pressure Gold Microneedling for the Treatment of Periorbital Wrinkles - A prospective Self-controlled Clinical Trial

Negative-pressure Gold Microneedling for the Treatment of Periorbital Wrinkles - A prospective Self-controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125605
Enrollment
Unknown
Registered
2026-05-28
Start date
2026-06-04
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

periorbital wrinkles

Interventions

Left side:Low-power long-pulse-width treatment method
Right side:High-power short-pulse-width treatment method

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients with periorbital wrinkles, with a Fitzpatrick wrinkle score of more than 3, aged between 25 and 65 years, regardless of gender. 2.Periorbital wrinkles have never undergone any other treatments. 3.After fully understanding the treatment plan and its risks, the individual or the guardian voluntarily signs the informed consent form, willing to participate in the self-controlled trial and cooperate with the follow-up.

Exclusion criteria

Exclusion criteria: 1.Pregnant women or women planning to conceive; 2.Those with severe dysfunction of the heart, liver and kidneys, autoimmune diseases, mental disorders or other major disorders of the body systems; 3.There are skin diseases such as traumatic, open wounds, suppurative wounds and active inflammatory herpes in the treatment area. 4.For those who are allergic to topical anesthetics or microneedle materials; 5.Patients currently participating in other clinical trials; 6.The treatment area has received phototherapy, injections, surgeries, etc. within the past one year. 7.Taking glucocorticoids or other immunosuppressants, or anticoagulants within one month; 8.The researchers considered those participants who were not suitable for the study.

Design outcomes

Primary

MeasureTime frame
severity of periorbital wrinkles;

Secondary

MeasureTime frame
Periorbital Wrinkles Area;severity and morphology of periorbital wrinkles;Subject satisfaction;TEWL;

Countries

China

Contacts

Public ContactLU Zhong

Huashan Hospital, Fudan University

2277@huashan.org.cn+86 21 5288 7765

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026