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Application of stem cell exosomes in facial rejuvenation treatment

Clinical study on the safety and effectiveness of stem cell exosomes in facial rejuvenation treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106710
Enrollment
Unknown
Registered
2025-07-29
Start date
2025-07-29
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Facial Aging?

Interventions

Test group:Stem cell exosomes

Sponsors

Shenzhen Qianhai Shekou Free Trade Zone Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Subject can read documents and voluntarily signs informed consent form. 2. Age 18~60 years old (inclusive), either gender. 3. The subject presents with static facial wrinkles, and according to the facial wrinkle assessment scale, any single wrinkle (glabellar lines, forehead lines, crow's feet, infraorbital wrinkles, nasolabial folds, and/or marionette lines) scores >=4 points.

Exclusion criteria

Exclusion criteria: 1. Muscular or nervous system diseases diagnosed clearly in the past, such as facial muscular atrophy, facial paralysis, etc.. 2. Patients who have undergone facial rejuvenation procedures? including but not limited to IPL, fractional laser treatment, mesotherapy, microneedling, and chemical peels within 3 months prior to enrollment?, or botulinum toxin injections, microfocused ultrasound, radiofrequency devices, or radiofrequency microneedling ?within 6 months prior to enrollment?. 3. Pregnant or lactating women, or male/female subjects planning pregnancy? (self or partner) ?within 6 months?. 4. Subjects with conditions significantly affecting efficacy evaluation? (e.g., conspicuous scars, hypertrichosis); 5. Suffering from systemic diseases, being on medication, or have been diagnosed with tumors. 6. Have dysfunction or failure of important organs. 7. Patients with a history of severe mental illness. 8. Patients with poor treatment compliance. 9. Have coagulation dysfunction or abnormal hematopoietic system. 10. Hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) positive, and HBV-DNA in peripheral blood is higher than the detection limit; Hepatitis C virus (HCV) antibody positive; Human immunodeficiency virus (HIV) antibody positive; Syphilis test antibody positive. 11. Patients deemed by the investigator to be ineligible for participation in this clinical study for any other reason.

Design outcomes

Primary

MeasureTime frame
Investigator subjective evaluation;Safety evaluation;Changes of skin physiological indexes;

Secondary

MeasureTime frame
Subject satisfaction;

Countries

China

Contacts

Public ContactHu Gang

Shenzhen Qianhai Shekou Free Trade Zone Hospital

hugangxa@163.com+86 755 2688 9440

Outcome results

None listed

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