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ClinicalTrials.gov record
Completed No phase listed Observational

Nodal Burden and Nodal Recurrence in Patients With Isolated Tumor Cells After Neoadjuvant Chemotherapy Treated With Axillary Dissection or Nodal Radiation: the OPBC-05/EUBREAST-14R/ICARO Study

ClinicalTrials.gov ID: NCT06464341

Public ClinicalTrials.gov record NCT06464341. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 2:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purposes of this multicenter retrospective cohort study are to determine the residual nodal burden in patients with isolated tumor cells detected in the SLN or the clipped node after NAC and to determine oncologic outcomes in this group of patients after ALND or nodal RT or observation.

Study identification

NCT ID
NCT06464341
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
583 participants

Conditions and interventions

Conditions

Interventions

Other

Eligibility (public fields only)

Age range
18 Years to 100 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 3, 2023
Primary completion
Dec 30, 2023
Completion
Dec 30, 2024
Last update posted
Jan 19, 2025

2023 – 2024

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Valleywise Health Medical Center Phoenix Arizona 85008
University of Southern California Los Angeles California 90033
Cedars-Sinai Medical Center, Samuel Oschin Cancer Institute Los Angeles California 90048
Miami University Miami Florida 33136
Dana Farber Cancer Institute Boston Massachusetts 02215
University of Michigan Ann Arbor Michigan 48109
Mayo Clinic Rochester Minnesota 55905
NYU Langone Health New York New York 10016
Memorial Sloan Kettering Cancer Center New York New York 10065
Weill Cornell Medical Center New York New York 10065
Montefiore Medical Center New York New York 10461
University of Rochester Rochester New York 14642
Duke University Durham North Carolina 27710
University of Pennsylvania Philadelphia Pennsylvania 19104
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213
Guthrie Clinic Sayre Pennsylvania 18840
The University of Texas, MD Anderson Cancer Center Houston Texas 77030
Swedish Cancer Institute Seattle Washington 98029
University of Washington Seattle Washington 98133

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06464341, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 19, 2025 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06464341 live on ClinicalTrials.gov.

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