Skip to content

Single-arm clinical trial of a medium-frequency electrotherapy device for facial rejuvenation

Single-arm clinical trial of a medium-frequency electrotherapy device for facial rejuvenation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127789
Enrollment
Unknown
Registered
2026-07-07
Start date
2025-07-02
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Facial aging

Interventions

Treatment:Medium-frequency electric stimulaiton with 70% to 100% intension, 30 minutes weekly for 4 weeks

Sponsors

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

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age between 35 and 70 years (inclusive), no restriction on sex; 2. Bilateral facial symmetry is generally normal; 3. Moderate to severe facial aging with FWS score >= 2; 4. No contraindications to electrical stimulation therapy; 5. Not engaged in outdoor occupations; 6. Good compliance as assessed by the investigator and able to complete follow-up visits; 7. Voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with a previously confirmed diagnosis of muscle or neurological disorders (e.g., facial muscle atrophy, facial paralysis, etc.); 2. Presence of metallic implants in the body (e.g., dental prostheses, cardiac pacemaker, artificial joints, etc.); 3. Pregnant or lactating women, or women planning to become pregnant within 6 months after completion of the study; 4. Skin diseases in the facial treatment area that may interfere with facial rejuvenation treatment or efficacy evaluation (e.g., eczema, allergic dermatitis, severe melasma, psoriasis, rosacea), or conditions such as obvious scarring or excessive facial hair that may significantly affect outcome assessment; 5. Participation in other clinical studies related to facial rejuvenation during the study period; 6. Patients unwilling to discontinue the use of other non-medical energy-based devices or unwilling to comply with sun protection requirements during the study period; 7. Patients who have received any facial rejuvenation treatments (e.g., medication, laser, intense pulsed light, RF, ultrasound, photodynamic therapy, etc.) within 4 weeks prior to enrollment; 8. Patients with concurrent systemic diseases, including but not limited to a history of cardiovascular disease, endocrine disorders (such as diabetes, dyslipidemia, thyroid dysfunction), hematologic diseases (such as anemia, coagulation disorders), or infectious diseases (such as herpes).

Design outcomes

Primary

MeasureTime frame
Response rate based on FWS decline index;

Secondary

MeasureTime frame
Patient satisfaction evaluation;Frontal muscle thickness increase index;GAIS score;

Countries

China

Contacts

Public ContactYao Min

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: Jul 23, 2026