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Effect of Adipose Derived Stem Cells on Survival of Fat as Filler

A

Alexandria University

Status

Completed

Conditions

Lipofilling
Skin Rejuvenation

Treatments

Procedure: lipofilling enriched with adipose tissue derived stem cells
Procedure: lipofilling

Study type

Interventional

Funder types

Other

Identifiers

NCT03965936
alexderma 2

Details and patient eligibility

About

this research is to study the effect of Adipose Derived Stem Cells on Survival of Fat as Filler

Full description

Skin aging is a complex biological process.The physiological changes associated with aging of the skin are manifested in xerosis, dramatic loss of skin elasticity due to damage to collagen and elastin fibers; as well as barrier function, modification of rhytides and deficiencies in the regenerative property of the skin. All of which ultimately result in thinning of the skin, malar fat atrophy and pigmentary changes. Autologous fat grafting or lipo injection containing stromal vascular fraction (SVF) acts like ideal soft tissue filler for facial filling and rejuvenation. It leads to progressive improvement of the skin texture, elasticity, and color over a few months, therefore adipose tissue seems to be not only a simple filler but also a dynamic filler with two types of different and supplementary effects, the volumetric effect and the regenerative effect.Cell assisted lipotransfer (CAL) is a technique that combines aspirated fat with concentrated ADSCs in the stromal vascular fraction (SVF) of the lipoaspirate. This technique could enhance the survival rate of the transplanted fat and leads to better cosmetic improvement

Enrollment

15 patients

Sex

Female

Ages

35+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  1. Clinically diagnosed facial skin aging.
  2. Glogau photoaging score II and III.
  3. Body mass index ≥20 with adequate abdominal or other subcutaneous adipose tissue accessible for lipoaspiration.

Exclusion Criteria:

  1. History of keloid formation.
  2. Any coincidental chronic illness (e.g. metabolic, autoimmune or endocrinal) or malignancy.
  3. Any bleeding or coagulation disorder or recent use of anticoagulant therapy.
  4. Active infection.
  5. History of any previous aesthetic procedure on the face within the past 6 months.
  6. History of intake of anti-aging systemic or topical medications within the previous 3 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

15 participants in 2 patient groups, including a placebo group

lipofilling
Placebo Comparator group
Description:
subcutaneous injection of lipoaspiate (microfat) in one temporal region
Treatment:
Procedure: lipofilling
lipofilling enriched with adipose tissue derived stem cells
Active Comparator group
Description:
subcutaneous injection of lipoaspiate enriched with adipose tissue derived stem cells in one temporal region
Treatment:
Procedure: lipofilling enriched with adipose tissue derived stem cells

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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