Skip to content

The study to evaluate the efficacy and safety of Polynucleotide on Acne Scars

The study to evaluate the efficacy and safety of Polynucleotide on Acne Scars

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230213003
Enrollment
27
Registered
2023-02-13
Start date
2023-02-13
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

Acne scar Polynucleotide, Acne scar

Interventions

Patients were treated with polynucleotide at acne scar for 3 sessions every 4 weeks. Then they were instructed to follow up at 1 month, 3 months, 6 months after the last treatments.
Experimental Device

Sponsors

SW HEALTHCARE CO.,LTD
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-60 years old 2. Both male and female 3. moderate to severe acne scar from global acne scar grading system

Exclusion criteria

Exclusion criteria: 1. Subjects who are pregnant 2. Subjects who had history of low platelet, coagulopathy or taking medicine of antocoagulant drug like warfarin 3. Subjects who has dermatits, wound or infection at treatment area 4. Subjects who allergy to anesthesia cream 5. Subjects who taken oral or injection contraceptive pills 6. Subjects who had history of laser, filler and botox at treatment area within 12 months before arrived the project 7. Subjects who had history of keloid or hypertrophic scar 8. Subjects who had history of psychitic disease 9. Subjects who use tretinoin or AHA with in 1 months

Design outcomes

Primary

MeasureTime frame
Average Wrinkle and Texture Baseline, 1 month after 1st treatment, 1 months after 2nd treatment, 1 month, 3 months, 6 months after the last treatments. Antera

Secondary

MeasureTime frame
Skin elasticity Baseline, 1 month after 1st treatment, 1 months after 2nd treatment, 1 month, 3 months, 6 months after the last treatments. Cutometer,Melanin index Baseline, 1 month after 1st treatment, 1 months after 2nd treatment, 1 month, 3 months, 6 months after the last treatments. mexameter,Erythema Index Baseline, 1 month after 1st treatment, 1 months after 2nd treatment, 1 month, 3 months, 6 months after the last treatments. Mexameter,Physician improvement scale Baseline, 1 month after 1st treatment, 1 months after 2nd treatment, 1 month, 3 months, 6 months after the last treatments. Percent improvement,Patient improvement scale Baseline, 1 month after 1st treatment, 1 months after 2nd treatment, 1 month, 3 months, 6 months after the last treatments. percent improvement,safety Baseline,1 month after 1st treatment, 1 months after 2nd treatment and 2 week, 1,2,3,6 months after 3rd treatments adverse effect

Countries

Thailand

Contacts

Public ContactRungsima Wanitphakdeedecha

Faculty of Medicine Siriraj Hospital, Mahidol University

rungsima.wan@mahidol.ac.th66816406300

Outcome results

None listed

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