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Absorbable Barbed Threads for Lower Facial Soft Tissue Repositioning in Asians

Absorbable Barbed Threads for Lower Facial Soft Tissue Repositioning in Asians

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210415001
Enrollment
38
Registered
2021-04-15
Start date
2019-12-25
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

Absorbable Barbed Threads for Lower Facial Lifting absorbable barbed threads, lower face lifting facial rejuvenation

Interventions

Absorbable Barbed Threads for Lower Facial Soft Tissue Repositioning
Experimental Procedure/Surgery
Absorbable Barbed Threads

Sponsors

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

Eligibility

Sex/Gender
Female
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: Male and female, between 30-55 years of age, with a maximum body mass index of 30 kg/m2 and mild to moderate facial laxity (1.5-2.5 points, according to a 4-point Quantitative Grading Scale for laxity),27 were included

Exclusion criteria

Exclusion criteria: patients who were pregnant or lactating; with a history of keloid or hypertrophic scar formation; a history of botulinum toxin, mesotherapy or laser treatment in the last 6 months; a history of filler injection in the last 12 months; concurrent dermatological disease, autoimmune disease or infection in the targeted area; currently using medications including antibiotics, anticoagulants, vitamin C or E supplementation, steroids, or nonsteroidal anti-inflammatory drugs (NSAID). Other exclusion criteria were a history of allergy to p(LA-CL), local anesthesia or adrenaline; a history of smoking; and patients who may not cooperate or comply with medical treatment requirements.

Design outcomes

Primary

MeasureTime frame
clinical improvement of facial laxity at 1-week, 1,2,3,6,12-month after end of the intervention graded by two blinded dermatologists

Secondary

MeasureTime frame
volume in the jawline, nasolabial folds and submental area at 1-week, 1,2,3,6,12-month after end of the intervention Vectra H1 Imaging System,Patient self-assessment at 1-week, 1,2,3,6,12-month after end of the intervention Patient self-assessment scores,adverse reactions at 1-week, 1,2,3,6,12-month after end of the intervention observed by dermatologists

Countries

Thailand

Contacts

Public ContactRungsima Wanitphakdeedecha

Department of Dermatology Faculty of Medicine Siriraj Hospital Mahidol University

rungsima.wan@mahidol.ac.th6624194333

Outcome results

None listed

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