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Active, not recruiting Not applicable Interventional

Partial Irradiation and Sequential vs. Concurrent Chemo Early Breast Cancer

ClinicalTrials.gov ID: NCT01928589

Public ClinicalTrials.gov record NCT01928589. 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 18, 2026, 6:16 AM EDT

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

Official title

Randomized Phase II Study of Partial Breast Irradiation and Sequential vs. Concurrent Chemotherapy in Women With Early Stage Breast Cancer (PBI 3.0)

Brief summary

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

In a small study at Johns Hopkins, women were treated with partial breast irradiation and chemotherapy given at the same time. We are now testing in a bigger study whether giving partial breast irradiation and chemotherapy at the same time (our new method) has the same side effects and outcomes as giving partial breast irradiation and chemotherapy at different times(older method). In this study women who had their breast cancer removed but need radiation to the breast will be randomized to partial breast irradiation at the same time as chemotherapy or partial breast radiation at a different time than chemotherapy. Randomization is like flipping a coin but in this study about 2 of every 3 women will get the new method.

Study identification

NCT ID
NCT01928589
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Richard Zellars
Other
Enrollment
81 participants

Conditions and interventions

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
Jan 15, 2014
Primary completion
Dec 11, 2023
Completion
Nov 30, 2028
Last update posted
Mar 5, 2026

2014 – 2028

United States locations

U.S. sites
10
U.S. states
5
U.S. cities
9
Facility City State ZIP Site status
Sibley Memorial Hospital Washington D.C. District of Columbia 20016
Parkview Regional Medical Center Fort Wayne Indiana 46845
Indiana University Health Hospital Indianapolis Indiana 46202
Indiana University Health Melvin and Bren Simon Comprehensive Cancer Center Indianapolis Indiana 46202
IU Health Arnett Lafayette Indiana 47905
John Hopkins University Baltimore Maryland 21218
Suburban Hospital Bethesda Maryland 20814
Reading Hospital West Reading Pennsylvania 19611
York Cancer Center York Pennsylvania 17403
University of Texas-San Antonio San Antonio Texas 78229

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01928589, 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 Mar 5, 2026 · Synced Sep 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01928589 live on ClinicalTrials.gov.

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