RECRUITING

Quantitative Assessment of Autologous Fat Transfer

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Quantitative Assessment of Autologous Fat Transfer

Quick Facts

Study Start:2024-01-25
Study Completion:2026-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06343831

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Planned autologous fat transfer or fat grafting reconstruction of the breast or chest wall.
  2. * Able to provide written or electronic informed consent.
  3. * Able to undergo MRI.
  1. * Vulnerable subjects (children, prisoners, pregnant women).
  2. * Patients who have active cancer, metastatic disease, solid organ transplantation / immunosuppression, or autoimmune diseases.
  3. * Unable to undergo MRI (history of metal contraindication, claustrophobia)

Contacts and Locations

Study Contact

Summer Hanson, MD
CONTACT
773-702-6302
sehanson@bsd.uchicago.edu

Principal Investigator

Summer Hanson, MD
PRINCIPAL_INVESTIGATOR
University of Chicago

Study Locations (Sites)

The University of Chicago
Chicago, Illinois, 60637
United States
The University of Houston
Houston, Texas, 77204
United States

Collaborators and Investigators

Sponsor: University of Chicago

  • Summer Hanson, MD, PRINCIPAL_INVESTIGATOR, University of Chicago

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-25
Study Completion Date2026-12

Study Record Updates

Study Start Date2024-01-25
Study Completion Date2026-12

Terms related to this study

Additional Relevant MeSH Terms

  • Autologous Fat Grafting