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A single-arm trial: simultaneous emission of synchronous radio frequency and high intensity focused electric field for non-invasive facial rejuvenation

A single-arm trial: simultaneous emission of synchronous radio frequency and high intensity focused electric field for non-invasive facial rejuvenation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077485
Enrollment
Unknown
Registered
2023-11-10
Start date
2023-11-12
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Facial aging

Interventions

Treatment:RF combined with HIFES

Sponsors

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) The patient is aged 30-70 years old, regardless of gender; (2) Bilateral facial symmetry; (3) Moderate to severe facial aging patients with FWS score = 4; (4) No contraindications for RF and electrical stimulation treatment; (5) Not outdoor professional workers; (6) Assess the patient's good compliance and be able to cooperate in completing follow-up; (7) Voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Muscle or nervous system diseases that have been diagnosed clearly in the past (such as facial atrophy, facial paralysis, etc.); (2) Metal implants in the body (such as dentures, pacemakers, artificial joints, etc.); (3) Pregnant women, lactating women, or women with a pregnancy preparation plan within six months after the end of the study; (4) The combination of facial treatment areas with other skin diseases that may interfere with the treatment or evaluation of facial rejuvenation (such as eczema, allergic dermatitis, severe melasma, psoriasis, rosacea, etc.), or scars, excessive hair, etc. that significantly affect the effectiveness of observation; (5) Participate in other clinical studies on facial rejuvenation during the study period; (6) Those who are unwilling to discontinue the stimulation of other non medical energy devices during the research period and do well in sun protection; (7) Those who have received any facial rejuvenation treatment (such as medication, laser, intense pulsed light, RF, ultrasound, photodynamic therapy, etc.) within the past 4 weeks before enrollment; (8) Complicated systemic diseases: including but not limited to cardiovascular disease history, endocrine diseases (such as diabetes, dyslipidemia, thyroid dysfunction, etc.), blood system diseases (such as anemia, abnormal coagulation mechanism, etc.) or infectious diseases (such as herpes, etc.).

Design outcomes

Primary

MeasureTime frame
Response rate based on FWS decline index;

Secondary

MeasureTime frame
Response rate based on FWS decline index;Response rate based on GAIS index;Patient satisfaction evaluation;

Countries

China

Contacts

Public ContactMin Yao

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine

my058@vip.sina.com+86 189 1779 7606

Outcome results

None listed

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