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Efficacy and safety of radiofrequency and focused ultrasound in facial rejuvenation:A Single-Center, Single-Blind, non-Randomized Prospective Trial

Efficacy and safety of radiofrequency and focused ultrasound in facial rejuvenation:A Single-Center, Single-Blind, non-Randomized Prospective Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097849
Enrollment
Unknown
Registered
2025-02-26
Start date
2023-11-03
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

aging

Interventions

radiofrequency group:Each participant received a single treatment of radiofrequency
focused ultrasound group :Each participant received a single treatment of focused ultrasound.

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: The study recruited patients aged between 25 and 55 years who had a need for facial rejuvenation.

Exclusion criteria

Exclusion criteria: Exclusion criteria included individuals who were pregnant or breastfeeding, those with implanted cardiac pacemakers or other similar electronic devices and metal implants, patients with other significant medical conditions, a history of anti-aging treatments within the last six months, individuals unable to cooperate, and those with poor adherence who could not follow up as scheduled.

Design outcomes

Primary

MeasureTime frame
Modified Fitzpatrick Wrinkle Scale;Facial Laxity Rating (FLR) Scale;Allergan Skin Roughness Scale(ASRS);VAS,Visual Analog Scale;—

Countries

China

Contacts

Public ContactShuping Hou

Tianjin Medical University General Hospital

housp_1978@163.com+86 138 2115 0956

Outcome results

None listed

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