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RECRUITING NA

Quantitative Assessment of Autologous Fat Transfer

NCT06343831 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • PROCEDURE 2-Dimensional (2-D) Photographs (Visit 1/ Follow up Visit 3-6)
  • PROCEDURE 3-Dimensional (3-D) Photographs (Visit 1- 6)
  • PROCEDURE Ultrasound Soft Tissue Assessment (Visit 1/ Follow up Visit 4-6)
  • PROCEDURE Magnetic Resonance Imaging Volume Assessment (Visit 1/ Follow up Visit 4-6)
  • PROCEDURE BREAST-QTM questionnaire (Visit 1/ Follow up Visit 4-6)

Study Locations (2)

Illinois

  • The University of Chicago — Chicago

Texas

  • The University of Houston — Houston

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2024-01-25
Est. Completion 2026-12
Phase NA

Sponsor

University of Chicago

846 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06343831

The ClinicalTrials.gov registry entry for NCT06343831 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 846 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Autologous Fat Grafting appearing as the primary indexed condition, and to 5 interventions — of which 2-Dimensional (2-D) Photographs (Visit 1/ Follow up Visit 3-6) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06343831 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Illinois, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06343831 about?

NCT06343831 is a clinical study titled "Quantitative Assessment of Autologous Fat Transfer". 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 p...

What is the current status of trial NCT06343831?

This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2024-01-25. Estimated completion is 2026-12.

What conditions does trial NCT06343831 study?

This clinical trial studies the following conditions: Autologous Fat Grafting. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06343831?

The interventions under investigation include: 2-Dimensional (2-D) Photographs (Visit 1/ Follow up Visit 3-6) (PROCEDURE), 3-Dimensional (3-D) Photographs (Visit 1- 6) (PROCEDURE), Ultrasound Soft Tissue Assessment (Visit 1/ Follow up Visit 4-6) (PROCEDURE), Magnetic Resonance Imaging Volume Assessment (Visit 1/ Follow up Visit 4-6) (PROCEDURE), BREAST-QTM questionnaire (Visit 1/ Follow up Visit 4-6) (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06343831?

This trial is sponsored by University of Chicago, which has 846 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06343831 being conducted?

This trial has 2 study locations across Illinois, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial