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Stem cell exosomes plus laser shows promise for stubborn melasma

NCT ID NCT06677931

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 treatment for melasma, a stubborn skin condition causing dark patches on the face. Researchers combined stem cell exosomes (tiny particles from umbilical cord cells) with a special laser in 30 adults. The goal was to see if this combo is safe and works better than laser alone. Results are being analyzed to see if it reduces pigmentation and repairs skin damage.

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

30 people

The number who actually took part.

Started

Aug 2024

Finished

Nov 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.

Ages

18 to 60 years

Sex

Anyone

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. Aged 18 to 60 years with good overall health. 2. Diagnosed with melasma according to clinical diagnostic criteria and efficacy standards (revised edition), with facial skin lesions. 3. Fully understands and comprehends the content and significance of the study, implementation plan, potential benefits, risks, mitigation measures, participant rights and obligations (including privacy protection and voluntary withdrawal), and willingly signs the informed consent form to participate in the clinical study, and can cooperate well. 4. Exclusion of inflammatory post-pigmentary disorders, malar melasma, Riehl's melanosis, pigmentary lichenoid dermatosis, and other skin diseases. 5. Agrees not to use other cosmetic treatments related to the study during the research period. Exclusion Criteria: 1. Patients who refuse to sign the informed consent form to participate in the trial. 2. History of significant organ diseases, autoimmune diseases, or immune dysfunction. 3. Abnormal coagulation function, current use of anticoagulants, tendency for thrombosis, or family history of genetic diseases. 4. Pregnant or lactating women. 5. Patients who have taken oral contraceptives or hormone replacement therapy during the study period or in the past 12 months. 6. Patients with a keloid-prone constitution. 7. Locally damaged or actively affected by other skin diseases. 8. History of severe multiple allergies, genetic allergies, photosensitivity or history of photosensitive drugs such as sulfonamides and tetracyclines, allergy to local anesthetics, lidocaine components, or planned desensitization therapy during the study. 9. History of post-inflammatory hyperpigmentation. 10. Previously treated for melasma. 11. Previous chemical peels, abrasion procedures, or other resurfacing treatments on the face. 12. Chronic skin diseases, especially infectious, allergic, and inflammatory systemic skin diseases such as widespread eczema, pemphigus, pemphigoid, etc. 13. Patients currently participating in other clinical studies. 14. Other reasons deemed unsuitable for the clinical study by the investigator.

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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

  • Affiliated Union Hospital of Fujian Medical University

    Fuzhou, Fujian, 350001, China

  • Chenxiaosong

    Fujian, Fuzhou, 350001, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.