Skip to content

The efficacy and safety of microfocused ultrasound combined with 633nm red light in reversing facial photoaging: A multicenter, prospective, randomized controlled study

The efficacy and safety of microfocused ultrasound combined with 633nm red light in reversing facial photoaging: A multicenter, prospective, randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092827
Enrollment
Unknown
Registered
2024-11-25
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Facial Tightening

Interventions

Group A:Half of the face was treated with microfocused ultrasound combined with 633nm red light
Group B:Half of the face was treated with 633nm red light

Sponsors

Shanghai Skin Disease Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male or female, aged 40-65 years old, who need to receive facial rejuvenation treatment due to facial aging; 2. Fitzpatrick skin type II-IV, with mild to severe facial aging manifestations, such as facial wrinkles, bilateral nasolabial folds, cheek skin laxity; 3. Agree to participate in this study and follow up on time by signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are pregnant, breastfeeding or planning to become pregnant during the follow-up period; 2. those with pre-existing keloids or proliferative scarring; 3. Those who are undergoing other clinical studies; 4. the presence of other skin diseases on the face that affect the evaluation of efficacy; 5. Those who have received phototherapy or topical epidermal regeneration drugs on the face within 1 month; 6. those who have received hyaluronic acid fillers, botulinum toxin treatment on the face within the previous 6 months or other facial treatments that may affect the evaluation of effectiveness; 7. those with severe systemic dermatologic diseases, medical disorders, coagulation disorders, psychological and psychiatric disorders, and infectious diseases; 8. other conditions that the investigator considers unsuitable for enrollment.

Design outcomes

Primary

MeasureTime frame
GAIS;

Secondary

MeasureTime frame
Wrinkle Score;Pigmentation Score;Adverse reaction assessment;Subject satisfaction;

Countries

China

Contacts

Public Contactxiuli Wang

Shanghai Skin Disease Hospital

xlwang2001@aliyun.com+86 21 6183 3081

Outcome results

None listed

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