Relationships between injectable hyaluronic acid filler for periorbital soft-tissue rejuvenation, self-esteem, quality of life and health behavior in women.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20210607004

Enrollment

Registered

2021-06-07

Start date

2020-10-01

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

Healthy female patients with periorbital aging Aesthetics, periorbital, dermal filler, self esteem, quality of life, health behavior

Interventions

1mL of Restylane SKINBOOSTERS VITAL LIGHT injectable hyaluronic acid filler for periorbital soft-tissue injection

Experimental Drug

Injectable hyaluronic acid filler

Eligibility

Sex/Gender

Female

Age

20 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age at least 20 years-old 2. Barton periorbital grade 1 2 and 3 3. Revised Thai RSES less than 31.02, and WHOQOL-BREF-THAI in psychological domain less than 23, social relationship domain less than 12, and overall less than 96 4. No contraindications for filler injection: allergy or hypersensitivity, pregnancy, lactation, local skin infection, post-vaccination in past 4wk, post-facial procedures in past 4wk, autoimmune diseases, malnutrition, psychiatric disorders 5. No conditions which might influence the intervention: prior facial filler injection in past 24 months, prior facial non-biodegradable filler injection, craniomaxillofacial implants, cheek and periorbital trauma or surgery, most of ophthalmologic disorders other than refractive errors 6. No conditions which might influence the quality of life: menopause, sleep disorders, disabilities, hypothyroidism and hyperthyroidism 7. Not a participant in other study 8. Ability to follow entire research methodology

Exclusion criteria

Exclusion criteria: 1. Any condition detected during the study that would render the patient unsuitable for the study 2. Do not meet inclusion criteria

Design outcomes

Primary

Measure	Time frame
Self-esteem before intervention and at 1, 3, and 6 months after end of the intervention Revised Thai Rosenberg self-esteem scale,Quality of life before intervention and at 1, 3, and 6 months after end of the intervention WHOQOL-BREF-THAI,Impact of periorbital aesthetic problem on quality of life before intervention and at 1, 3, and 6 months after end of the intervention Periorbital aesthetic life quality index	—

Measure

Time frame

Self-esteem before intervention and at 1, 3, and 6 months after end of the intervention Revised Thai Rosenberg self-esteem scale,Quality of life before intervention and at 1, 3, and 6 months after end of the intervention WHOQOL-BREF-THAI,Impact of periorbital aesthetic problem on quality of life before intervention and at 1, 3, and 6 months after end of the intervention Periorbital aesthetic life quality index

—

Secondary

Measure	Time frame
Periorbital aging before intervention, immediately after the intervention, and at 1, 3, and 6 months after end of the intervention Barton grading system for periorbits,Health bahavior before intervention and at 1, 3, and 6 months after end of the intervention Health bahavior questionnaire	—

Countries

Thailand

Contacts

Public ContactPeerapong Jiamjirachart

THE CAPITAL CLINIC Co., Ltd.

DIRTGENE@gmail.com0828800973

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026