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Efficacy evaluation of negative pressure fractional radiofrequency microneedle in periorbital rejuvenation

Efficacy evaluation of negative pressure fractional radiofrequency microneedle in periorbital rejuvenation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057920
Enrollment
Unknown
Registered
2022-03-22
Start date
2022-03-11
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

periorbital rejuvenation

Interventions

Group 1 :Negative pressure fractional microneedle radiofrequency

Sponsors

Chengdu Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 35-65 years; 2. Fitzpatrick skin type III-IV; 3. It meets the diagnostic criteria of periorbital aging: periorbital skin laxity, eyelid ptosis and obvious wrinkles; 4. No treatment history of periorbital skin aging in recent half a year, such as laser, injection and orbital plastic surgery, etc.; 5. Patients who are willing to perform radiofrequency microneedle treatment with negative pressure lattice around orbit.

Exclusion criteria

Exclusion criteria: 1. Open facial trauma, infected persons; 2. Patients with severe endocrine diseases or cardiovascular diseases; 3. Previous history of mental illness, alcoholism and drug addiction; 4. Scar constitution; 5. Pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Visia wrinkle area Value;Skin mirror;Skin biopsy;

Countries

China

Contacts

Public ContactWa Qingbiao

Chengdu Second People's Hospital

295615394@qq.com+86 13981987190

Outcome results

None listed

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