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New laser zaps freckles just as well as old one, study finds

NCT ID NCT07352631

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a new laser device for removing freckles on the face. 84 Chinese adults with freckles on both cheeks received one treatment with the new laser on one side of their face and an approved laser on the other. After 8 weeks, doctors compared how much the freckles faded and checked for side effects. The goal was to see if the new laser works as well and is as safe as the approved one.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

84 people

The number who actually took part.

Started

Dec 2024

Finished

Aug 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Aged 18 to 65 years (inclusive). * Fitzpatrick skin type III, IV, or V. * Diagnosed with facial freckles. * Presence of visually symmetrical bilateral facial freckles. * Able to understand and voluntarily sign the informed consent form. * Willing and able to comply with all study procedures and follow-up visits. Exclusion Criteria: * High photosensitivity to any light spectrum. * Severe organic diseases (e.g., epilepsy, psychosis). * History of sunburn within the past 1 month. * History of skin malignancies (e.g., squamous cell carcinoma, melanoma). * Skin lesions that are broken, inflamed, or with a history of poor wound healing or keloids. * Diagnosis of cutaneous lupus erythematosus. * Significant systemic disease or obvious lesions in the treatment area. * Presence of herpes simplex virus (HSV) in the expected treatment area. * Active local or systemic infection, or open wounds in the treatment area. * History of immunosuppression/immunodeficiency (including HIV/AIDS) or use of immunosuppressive drugs. * Use of anticoagulants or medications that may alter wound healing within the past 1 month. * Use of known photosensitizing medications within the past 1 month. * Oral isotretinoin (Accutane) use within 12 months prior to initial treatment or planned use during the study. * Use of iron supplements, herbal supplements (e.g., Ginkgo, Ginseng, Garlic), or fish oil supplements within the past 1 month. * Other photo or energy-based aesthetic procedures in the treatment area within the past 1 month. * Pregnancy, lactation, or planning pregnancy during the study period. * Participation in another clinical trial (except registry studies) within 3 months prior to screening. * Considered by the investigator to have poor compliance or otherwise unsuitable for participation.

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Conditions

The condition(s) this trial relates to.

Melanosis

As listed by the trial registrant

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

Contacts and locations

Locations

  • Beijing Hospital

    Beijing, China

  • Bengbu First People's Hospital

    Bengbu, Anhui, China