None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy volunteers over aged 30 years with facial volume loss scale 2 or 3 grade
Exclusion criteria
Exclusion criteria: 1) Patients with severe chronic wasting disease 2) Patients with impaired blood clotting 3) Pregnancy, breastfeeding women who are pregnant or plan for a trial period 4) Patients with infectious skin disease on the face 5) When receiving the treatments that can affect the shape and volume of the latest face within 6 months 6) During the trial period, other cosmetic procedure if you have planned 7) Persons who are participating in other clinical studies 8) Communication is impossible or difficult to follow the instructions 9) Not suitable for this trial under tester decision
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Facial volume loss scale, Objective volume change with Vectra | — |
Secondary
| Measure | Time frame |
|---|---|
| Facial volume change with different injection schedules | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital