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An exploratory study on the clinical efficacy of facial and neck rejuvenation with 3D digital plastic scanner.

An exploratory study on the clinical efficacy of facial and neck rejuvenation with 3D digital plastic scanner. - Evaluation of the efficacy of facial neck rejuvenation with 3D plastic scanner

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078757
Enrollment
Unknown
Registered
2023-12-18
Start date
2023-12-30
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Facial and neck aging

Interventions

Trail group:NA

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Patients treated in Dermatology department of Peking University Shenzhen Hospital for facial and neck rejuvenation ? Age range: 25-60 years old ? Subjects have good compliance, can fully understand the clinical trial, and can follow the study procedures until the end of the clinical trial ? Subjects fully understand the requirements of the trial, and voluntarily sign informed consent

Exclusion criteria

Exclusion criteria: ?Participants screened for additional facial-neck treatment within the preceding 6 months or planned to receive additional facial-neck treatment during the study. (such as facial lift, lipopolysis, laser resurfacing, rejuvenation, intense pulse light, RF, grinding, chemical stripping, any type of injection filling) ? Any manual or oral procedure that may induce significant changes (=10%) in body redevelopment is planned during the study period Drugs that may induce significant (=10%) changes (e.g., systemic corticosteroids, diet drugs, bariatric surgery) ? participation in any other clinical trial within 3 months prior to screening ?There are other co-morbidities that only the investigator believes may interfere with the study evaluation, or the investigator believes that participation in the study may result in subjects being at greater risk ?Subjects deemed unfit to participate in the study

Design outcomes

Primary

MeasureTime frame
Facial and neck structure;

Secondary

MeasureTime frame
Lower face volume;

Countries

China

Contacts

Public ContactXingling Jian

Peking University Shenzhen Hospital

329248192@qq.com+86 136 6228 7758

Outcome results

None listed

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