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The study to evaluate the efficacy and safety of Adjustable-depth fractional microneedle bipolar radiofrequency in Treatment of Wrinkle and Facial Contouring

The study to evaluate the efficacy and safety of Adjustable-depth fractional microneedle bipolar radiofrequency in Treatment of Wrinkle and Facial Contouring

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230331003
Enrollment
28
Registered
2023-03-31
Start date
2023-03-21
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 patient Adjustable-depth fractional microneedle bipolar radiofrequency,Wrinkle and Facial Contouring

Interventions

Patients were treated with Morpheus8 for 1 session then they were instructed to follow up at 1 month, 3 months, 6 months after the last treatments.
Experimental Device

Sponsors

ASTRACO MEDICAL NETWORKS LTD.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Aged 25-55 years 2. Both male and Female 3.mild to moderate skin laxity

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 melasma treatment within 6 months before arrived the project 7. Subjects who had history of laser at treatment area within 6 months before arrived the project 8. Subjects who had history of keloid or hypertrophic scar 9. Subjects who had history of psychitic disease

Design outcomes

Primary

MeasureTime frame
Volume change Baseline, 1 month,3 months, 6 months Vectra

Secondary

MeasureTime frame
Skin Texture and Wrinkle Baseline, 1 month,3 months, 6 months Antera,Doctor evaluation 1 month,3 months, 6 months Quatile scale,Patient evaluation 1 month,3 months, 6 months Quatile scale,Pain score 1 month,3 months, 6 months Visual analog scale,safety 1 month,3 months, 6 months Adverse effect

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 9, 2026