Healthy human volunteers Botulinum Toxins, Injections, Intradermal
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy male or female volunteers age 25-45 years, 2. No history of botulinum toxin treatment failure, 3. No history of immunodeficiency disease or taking any immunosuppressive drug, 4. Have facial sagging
Exclusion criteria
Exclusion criteria: 1. pregnant or lactating woman, 2. Was treated with botulinum toxin during 6 months prior, 3. Having the skin disease around the treated area 4. Using an energy-based device or other interventions 6 months prior
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Facial sagging improvement Before intervention, 14 days, 1, 2, 3, 4, 5 and 6 months after the intervention Level of improvement measure from vectra3d scan,Subject self assessment score 14 days, 1, 2, 3, 4, 5 and 6 months after the intervention percentage of Subject self assessment score,Physicians assessment score 14 days, 1, 2, 3, 4, 5 and 6 months after the intervention percentage of Physicians assessment score | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain score immediate after the intervention Visual analogue scale (0-10) | — |
Countries
Thailand
Contacts
Faculty of Medicine Siriraj Hospital, Mahidol University