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OpenTrials
Completed

NCT Number: NCT04896437

Direct Use of Non-centrifuged Autologous Fat Graft

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.

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Key information

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Observational

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diabetic,
  • venous
  • traumatic wounds

Exclusion criteria

  • Malignancy,
  • A life expectation <1 year,
  • Chemical or radiation exposure.
  • Pregnancy

Treatment and study plan

non-centrifuge fat graft application to the wounds

Procedure

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.

Primary outcomes

  1. Wounds examination

    Time frame: 6 months

    Collection 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 outcomes

  1. Wounds classification according to data from files and photographs

    Time frame: 3 months

    In this season the data will be classified according to the wounds parameters and photograph

  2. Final evaluation and data achieving from files and exam carts

    Time frame: 3 months

    all data will be examined and evaluated whether there is any difference between probable groups

Sponsors and collaborators

Lead sponsor

Samsun Liv Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2019
Study completion
2020
First posted
May 21, 2021
Registry last updated
May 21, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.