Phase
Condition
N/ATreatment
Placebo Comparator:1565 non-ablative fractional laser combined with normal Saline
1565 non-ablative fractional laser combined with umbilical cord mesenchymal stem cell-derived exosomes.
Clinical Study ID
Ages 18-60 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Aged 18 to 60 years with good overall health.
Diagnosed with melasma according to clinical diagnostic criteria and efficacystandards (revised edition), with facial skin lesions.
Fully understands and comprehends the content and significance of the study,implementation plan, potential benefits, risks, mitigation measures, participantrights and obligations (including privacy protection and voluntary withdrawal), andwillingly signs the informed consent form to participate in the clinical study, andcan cooperate well.
Exclusion of inflammatory post-pigmentary disorders, malar melasma, Riehl'smelanosis, pigmentary lichenoid dermatosis, and other skin diseases.
Agrees not to use other cosmetic treatments related to the study during the researchperiod.
Exclusion
Exclusion Criteria:
Patients who refuse to sign the informed consent form to participate in the trial.
History of significant organ diseases, autoimmune diseases, or immune dysfunction.
Abnormal coagulation function, current use of anticoagulants, tendency forthrombosis, or family history of genetic diseases.
Pregnant or lactating women.
Patients who have taken oral contraceptives or hormone replacement therapy duringthe study period or in the past 12 months.
Patients with a keloid-prone constitution.
Locally damaged or actively affected by other skin diseases.
History of severe multiple allergies, genetic allergies, photosensitivity or historyof photosensitive drugs such as sulfonamides and tetracyclines, allergy to localanesthetics, lidocaine components, or planned desensitization therapy during thestudy.
History of post-inflammatory hyperpigmentation.
Previously treated for melasma.
Previous chemical peels, abrasion procedures, or other resurfacing treatments on theface.
Chronic skin diseases, especially infectious, allergic, and inflammatory systemicskin diseases such as widespread eczema, pemphigus, pemphigoid, etc.
Patients currently participating in other clinical studies.
Other reasons deemed unsuitable for the clinical study by the investigator.
Study Design
Study Description
Connect with a study center
Affiliated Union Hospital of Fujian Medical University
Fuzhou, Fujian 350001
ChinaActive - Recruiting
Chenxiaosong
Fujian, fuzhou 350001
ChinaActive - Recruiting
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