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Ultrasound Face-Lift study shows promise for firmer skin

NCT ID NCT06286384

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether microfocused ultrasound can tighten aging facial skin. Thirty adults aged 25 to 60 with sagging skin and wrinkles received the treatment. Researchers used 3D imaging to measure changes in nasolabial folds, cheek volume, and brow height over 180 days. The goal was to see if the procedure is safe and effective for facial rejuvenation.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

30 people

The number who actually took part.

Started

Jul 2023

Finished

Mar 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Healthy women who age naturally

Ages

25 to 60 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Ages between 25 and 60 years old. 2. Clear manifested skin issues such as sagging and wrinkles: Merz Facial Aesthetics Score of 2 or above. 3. Absence of significant systemic diseases, cardiovascular disorders, impaired liver or kidney function, malignant tumors, etc. 4. Willing to participate in this study and sign an informed consent form. Exclusion Criteria: 1. Pregnant or lactating women. 2. Individuals with a scar-prone constitution, allergic or abnormally healing skin. 3. Treatment areas with damaged skin, acute inflammation, active infection, rosacea, vitiligo in the progressive stage, or severe acne. 4. Patients with skin conditions such as urticaria, itching, or other dermatological diseases. 5. Those with psychological disorders or drug allergies. 6. Individuals harboring unrealistic expectations about treatment outcomes. 7. Treatment areas containing metal foreign bodies or fillers deemed unsuitable for treatment by the physician. 8. Recent facial laser treatments or injections within the past month, including but not limited to filler treatments such as hyaluronic acid, botulinum toxin, and PRP injection therapy. 9. Any skin-tightening cosmetic treatments on the face or neck within the last three months. 10. Any minimally invasive cosmetic treatments on the face within the last three months. 11. Thread embedding treatments on the face within the last year, excluding thread blepharoplasty. 12. Patients with severe insomnia or those requiring intense sun exposure within the next three months. 13. Patients deemed unsuitable for participation by the investigator. 14. Those unable to cooperate with the treatment and complete all required visits.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • First Affiliated Hospital of Jinan University

    Guangzhou, Guangdong, 510000, China

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