The science behind autologous fat grafting.
Elisa Bellini, Michele P Grieco, Edoardo Raposio
https://pubmed.ncbi.nlm.nih.gov/29188051Actively Recruiting
Led by CERM INC. · Updated on 2025-05-31
40
Participants Needed
2
Research Sites
13 weeks
Total Duration
Researchers are evaluating Autologous Adipose Cell Therapy to improve skin rejuvenation and hair restoration. This therapy aims to overcome the limitations of traditional fat grafting and dermal fillers by isolating early-stage fat cells for better distribution and longer-lasting effects. The study focuses on assessing the safety, feasibility, and effectiveness of this therapy for conditions like wrinkles, fine lines, skin elasticity loss, pigmentation, hair thinning, and hair loss. Participants will receive the Autologous Adipose Cells therapy treatment, which involves processing fat cells from their own body to enhance skin and hair appearance. The therapy is monitored by the primary investigator for up to 25 weeks to evaluate outcomes. This study includes only one treatment group receiving this biological intervention. During the study, participants will undergo various assessments including imaging, satisfaction surveys, and evaluation reports from the first visit before treatment through the last follow-up visit between weeks 16 and 25. The plastic surgeon will monitor treatment effects and safety over a six-month period. The total involvement spans from initial treatment to multiple follow-ups to track skin and hair improvements and participant satisfaction.
CONDITIONS
Autologous Adipose Cells Therapy
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Treatment duration not explicitly specified; safety and efficacy monitored up to 25 weeks after treatment.
Participants receive Autologous Adipose Cells therapy treatment.
Multiple visits for treatment and monitoring over up to 25 weeks
Duration - Up to 25 weeks after treatment
Participants are monitored and evaluated by the primary investigator for treatment outcomes including safety, efficacy, and participant satisfaction.
Regular follow-up visits from week 16 to week 25
Total: 2 locations
1
The Centre for Cosmetic Surgery & Medicine, Newark
Lewes, Delaware, United States, 19958
Actively Recruiting
2
The Centre for Cosmetic Surgery & Medicine
Newark, Delaware, United States, 19713
Actively Recruiting
A
Ankeet Dixit
W
Wing Nam Fung
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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