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Anti aging efficacy of radiofrequency system of Beaty skin device

Evaluation of the efficiency and safety of the RF Fractional microneedling system of Beaty skin device made by Faragard Fanavari Company in rejuvenating and improving the signs of aging facial skin

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190210042676N11
Enrollment
20
Registered
2020-11-18
Start date
2020-05-21
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

None listed

Interventions

Intervention group: 2 sessions of full face treatment with RF Fractional microneedling probe of Beauty skin device. intensity 7 out of 10, active puls count 200 --250, depth 1 mm and time interval 1.5

Sponsors

Fanavari Faragard Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: mild to moderate wrinkles or sagging facial skin based on Glogau scale Signing the consent form for participation in the study

Exclusion criteria

Exclusion criteria: History of any implant placement including silicone, fat, collagen, hyaluronic acid or synthetic materials on face History of using RF during the past year History of Botox injection in face within the past 6 months Isotretinoin use in the last 6 months Active smoker in last 2 years Pregnancy or lactating

Design outcomes

Primary

MeasureTime frame
?acial skin wrinkle grading, using Glogau scale. Timepoint: Before intervention and 1 and 8 weeks after last treatment session. Method of measurement: One independent dermatologist will perform clinical assessments using patients’ photographs according to the Glogau scale.;Skin elasticity. Timepoint: Before intervention and 1 and 8 weeks after last treatment session. Method of measurement: Cutometery.

Secondary

MeasureTime frame
Skin thickness and density. Timepoint: Before intervention and 1 and 8 weeks after last treatment session. Method of measurement: Skin ultrasound.;Area and volume of nasolabial fold. Timepoint: Before intervention and 1 and 8 weeks after last treatment session. Method of measurement: VisioFace camera.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAniseh Samadi

Tehran University of Medical Sciences

aniseh_samadi@yahoo.com+98 21 8896 0880

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026