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Acellular Dermal Matrix Investigation in Breast Reconstruction
NCT06456554 · View on ClinicalTrials.gov ↗
Study Summary
Prospective, multi-center, dual-arm non-randomized clinical study in females undergoing a two-stage breast reconstruction using a pre-pectoral technique.
Conditions Studied
Interventions
- DEVICE Acellular Dermal Matrix (Cortiva Tissue Matrix)
Study Locations (10)
Missouri
- Washington University — St Louis
- Mercy Hospital — St Louis
New York
- NYU Langone Health — New York
- New York Presbyterian Hospital/Columbia University Irving Medical Center — New York
Arkansas
- University of Arkansas — Little Rock
California
- City of Hope National Medical Center — Duarte
Colorado
- University of Colorado — Aurora
Ohio
- Cleveland Clinic — Cleveland
Oklahoma
- Mercy Hospital — Oklahoma City
Pennsylvania
- University of Pennsylvania — Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 467 participants |
| Start Date | 2024-11-22 |
| Est. Completion | 2027-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06456554
The ClinicalTrials.gov registry entry for NCT06456554 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 467 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is RTI Surgical, which has 4 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 Breast Reconstruction appearing as the primary indexed condition, and to 1 intervention — of which Acellular Dermal Matrix (Cortiva Tissue Matrix) 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: NCT06456554 reports 10 study locations spanning 8 distinct geographic areas — top geographies include Missouri, New York, Arkansas. 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 NCT06456554 about?
NCT06456554 is a clinical study titled "Acellular Dermal Matrix Investigation in Breast Reconstruction". Prospective, multi-center, dual-arm non-randomized clinical study in females undergoing a two-stage breast reconstruction using a pre-pectoral technique.
What is the current status of trial NCT06456554?
This trial is currently recruiting. It is a NA study. The enrollment target is 467 participants. The study started on 2024-11-22. Estimated completion is 2027-12.
What conditions does trial NCT06456554 study?
This clinical trial studies the following conditions: Breast Reconstruction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06456554?
The interventions under investigation include: Acellular Dermal Matrix (Cortiva Tissue Matrix) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06456554?
This trial is sponsored by RTI Surgical, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06456554 being conducted?
This trial has 10 study locations across Arkansas, California, Colorado, Missouri, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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