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The study to evaluate the efficacy and safety of using hyaluronic acid filler for facial lifting in Thailand

The study to evaluate the efficacy and safety of using hyaluronic acid filler for facial lifting in Thailand

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250217009
Enrollment
25
Registered
2025-02-17
Start date
2023-11-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Facial skin laxity Skin laxity, hyaluronic acid filler, facial lifting

Interventions

Patients were injected with hyaluronic acid filler for total 3.3 ml once. Then they were instructed to follow up at immediate, 1, 3, 6, 9 and 12 months after the treatment.
Experimental Drug

Sponsors

Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. aged 30-55 years 2. were diagnosed with mild to moderate skin laxity

Exclusion criteria

Exclusion criteria: 1. Patients who are pregnant or lactating 2. Patients with dermatitis, open wound, or having infection at the area of face 3. Patients who underwent facial lifting within 6 months 4. Patients with serious underlying diseases 5. Patients who received filler injection or thread lift within 12 months 6. Patients who received botulinum toxin injection within 6 months 7. Patients with keloid scar 8. Patients with mental disorders 9. Patients who do not allow photography 10. Patients who received immunosuppressive drugs (e.g. steroids), chemotherapy or Aspirin 11. Patients with history of local anasthesia or hyaluronic acid allergy

Design outcomes

Primary

MeasureTime frame
Volume change by Vectra Baseline, immediate, 1, 3, 6, 9, 12 months Vectra

Secondary

MeasureTime frame
Physician improvement scale Immediate, 1, 3, 6, 9, 12 months Quartile scale ,Patient improvement scale Immediate, 1, 3, 6, 9, 12 months Quartile scale,Safety Immediate, 1, 3, 6, 9, 12 months Adverse event

Countries

Thailand

Contacts

Public ContactThanya Techapichetvanich

Faculty of Medicine Siriraj Hospital, Mahidol University

thanya.tec@gmail.com66837122248

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026