Skip to content

Preliminary Study on the Promotion of Facial Rejuvenation Using Exosomes Derived from Human Adipose Tissue

Preliminary Study on the Promotion of Facial Rejuvenation Using Exosomes Derived from Human Adipose Tissue

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117991
Enrollment
Unknown
Registered
2026-01-30
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Skin aging

Interventions

control group:Only basic hydrating injection
AT- EV group:A composite preparation of fat tissue-derived exosomes and basic mesotherapy solution for superficial facial skin injection

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 25 and 55 years (inclusive), regardless of gender. 2.Mild to moderate facial aging (such as Glogau grade II-III), with no severe skin lesions (such as active dermatitis, infections, etc.). 3.No aesthetic medical treatments (such as laser, injectable fillers, etc.) in the past 3 months, and no use of medications affecting skin function in the past 4 weeks. 4.Understand and agree to the study requirements, voluntarily sign the informed consent form, and be able to complete all follow-up and assessments. 5.Non-pregnant and non-lactating women, with no plans for pregnancy during the study period. 6.Non-smokers or light smokers (=5 cigarettes per day).

Exclusion criteria

Exclusion criteria: 1.The participant has uncontrolled systemic diseases (such as cardiovascular disease, diabetes, malignancies). 2.The participant has immune system diseases or an immunosuppressive state (such as lupus, post-organ transplantation reactions). 3.The participant has severe skin conditions on the face (such as active dermatitis, infections, keloids). 4.The participant has severe mental health disorders, such as depression, anxiety, etc. 5.The participant has a history of prolonged, high-intensity sun exposure in the past 3 months (such as outdoor workers, frequent sunbathers, etc.). 6.The participant has previously participated in another interventional study, and the study ended less than 3 months ago.

Design outcomes

Primary

MeasureTime frame
Improvement in skin elasticity and pigmentation.;

Countries

China

Contacts

Public ContactKai Liu

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

drkailiu@126.com+86 21 2327 1699

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026