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Autologous Fat Grafting clinical trials

View clinical trials related to Autologous Fat Grafting.

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NCT ID: NCT06343831 Not yet recruiting - Clinical trials for Autologous Fat Grafting

Quantitative Assessment of Autologous Fat Transfer

Start date: April 2024
Phase: N/A
Study type: Interventional

This is a single-arm, prospective pilot study that will objectively assess outcomes in patients electively undergoing Autologous Fat Transfer (AFT) for breast or chest wall reconstruction. Patients planning to undergo autologous fat transfer for breast or chest wall reconstruction will be enrolled prospectively. Participants will undergo standard photographs (2-D imaging) of their chest wall and torso, including the breasts, and complete a validated questionnaire (BREAST-QTM) to evaluate patient satisfaction, and quality of life, all standard of care. The 3D photographs, Magnetic resonance imaging (MRI), and Ultrasound (US) are routinely used in practice but will be performed for research purposes in this study. All imaging procedures and questionnaires will be obtained at baseline and follow-up visits 3-6.

NCT ID: NCT04906811 Terminated - Clinical trials for Autologous Fat Grafting

Prospective Comparison of Revolve™ and AuraGen 123 With AuraClens™ in Autologous Fat Grafting to the Breast

Start date: May 20, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare fat graft retention over time from lipoaspirate processed using two FDA-cleared devices: the Revolve System (K120902) and the AuraGen 1-2-3 with AuraClens Lipoaspirate Wash System (BK190433).

NCT ID: NCT03544593 Recruiting - Clinical trials for Autologous Fat Grafting

The Volumetric Analysis of Fat Grafting

Start date: January 4, 2018
Phase: N/A
Study type: Interventional

Title: The Volumetric Analysis of Fat Grafting for Aesthetic Body Contouring. Subjects who wish to undergo fat grafting for aesthetic body contouring will be offered enrollment to the study. The study will consist of a Screening/Baseline visit, Surgery day and 3 follow up visits. Each follow up visit will utilize Vectra 3D photography (Canfeild, NJ) to collect volumetric data. At the conclusion of the study, Volume data from Baseline and 3 follow up visits will be analyzed to determine fat retention rates.

NCT ID: NCT01750424 Withdrawn - Clinical trials for Autologous Fat Grafting

3-D Imaging Assessment of Scar Formation and Would Healing in Fat Grafted vs Non-Fat Grafted Facial Reconstruction Wound Sites

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess scar-formation and wound healing following the use of autologous fat grafting in facial reconstruction patients. Patients who have undergone facial reconstruction in the last 3 months will be randomized into two groups, one receiving fat grafting and one not receiving any intervention. These patients will continue to follow-up in our clinic for one year, with 3-D images taken at each follow-up visit to assess scar formation and wound healing. Assessment of the scar will be undertaken by both healthcare personnel as well as general lay public. We hypothesize that patients undergoing fat grafting to the wound site will achieve a more aesthetically appealing result, with less scarring and improved wound healing as judged by both the general public and healthcare professionals.