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Direct Use of Non-centrifuged Autologous Fat Graft

Direct Use of Autologous Fat Graft on The Treatment of Lower Extremity Wounds

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04896437
Enrollment
16
Registered
2021-05-21
Start date
2016-03-02
Completion date
2020-03-18
Last updated
2021-05-21

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

Conditions

Wound Healing Delayed

Keywords

diabetic food, lower extremity, fat graft, nonentrifuged

Brief summary

There are a limited number of reports related to the direct use of non-centrifuged adipose tissue graft in the literature. This preliminary study aims to present our experience on the efficacy of autologous fat graft use without centrifuging in the treatment of lower extremity wounds.

Detailed description

16 wounds treated with non-centrifuged autologous fat grafts were included in the study. The data were retrospectively analyzed. VAC (vacuum-assisted therapy) or silver-impregnated dressing was used to achieve a healthy wound bed before fat grafting. Autologous fat grafts were harvested from abdominal or gluteal regions of the patients and injected into the wound bed and wound environment. Clinical observation and photograph records were used to follow the wounds.

Interventions

PROCEDUREnon-centrifuge fat graft application to the wounds

Autologous fat grafts were harvested from abdominal or gluteal regions of the patients and injected into the wound bed and wound environment. Clinical observation and photograph records were used to follow the wounds.

Sponsors

Samsun Liv Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. diabetic, 2. venous 3. traumatic wounds

Exclusion criteria

1. Malignancy, 2. A life expectation \<1 year, 3. Chemical or radiation exposure. 4. Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Wounds examination6 monthsCollection of the data from clinical observation and photograph records were made to follow the wounds. the observations were made during changing the wound dressing and generally every three days.

Secondary

MeasureTime frameDescription
Wounds classification according to data from files and photographs3 monthsIn this season the data will be classified according to the wounds parameters and photograph
Final evaluation and data achieving from files and exam carts3 monthsall data will be examined and evaluated whether there is any difference between probable groups

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026