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Clinical control study and safety evaluation of the therapeutic effect of soluble hyaluronic acid microneedle and non-ablative fractional laser on periorbital wrinkles

Clinical control study and safety evaluation of the therapeutic effect of soluble hyaluronic acid microneedle and non-ablative fractional laser on infraorbital wrinkles

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046497
Enrollment
Unknown
Registered
2021-05-16
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

Wrinkles

Interventions

Group A:Non-ablative fractional laser
Group B:Soluble hyaluronic acid microneedle

Sponsors

Shanghai Skin Disease Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients of 18-65 years old; 2. Infraorbital wrinkles assessment standard score 3 points and above; 3. Meet the static crow's feet grading standard 3 and above; 4. Voluntarily sign an informed consent to participate in the clinical trial.

Exclusion criteria

Exclusion criteria: 1. Those who are known to be allergic to test drugs or related drugs; 2. Pregnant or lactating women; 3. Received wrinkle treatment (laser, radio frequency, fruit acid, photon, hyaluronic acid filling, etc.) within 6 months before enrollment; 4. Those who have other diseases (infection, dermatitis, sunburn, scars, etc.) that may affect the evaluation of the efficacy of the facial treatment area and nearby areas; 5. Received anti-inflammatory, glucocorticoid or tretinoin treatment within 1 month before enrollment; 6. Participate in any drug clinical trial (as a subject) within 1 month before participating in this trial; 7. Combined with serious diseases, including severe heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled high blood pressure, etc.; 8. Those with scar constitution; 9. Subjects with severe physical or mental illness that the investigator believes may affect treatment, evaluation, or poor compliance with the research protocol.

Design outcomes

Primary

MeasureTime frame
VISIA photos of wrinkles;

Secondary

MeasureTime frame
side effects;

Countries

China

Contacts

Public ContactWang Xiuli

Shanghai Skin Disease Hospital

wangxiuli_1400023@tongji.edu.cn+86 18017336663

Outcome results

None listed

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