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Completed Phase 2 Interventional Results available

Accelerated Partial Breast Radiation Therapy Using High-Dose Rate Brachytherapy in Treating Patients With Early Stage Breast Cancer After Surgery

ClinicalTrials.gov ID: NCT02526498

Public ClinicalTrials.gov record NCT02526498. 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 8, 2026, 10:23 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

TRI-fraction Radiotherapy Utilized to Minimize Patient Hospital Trips : A Phase II Trial (TRIUMPH-T Trial)

Brief summary

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

This phase II trial studies how well accelerated partial breast irradiation (APBI) using high-dose rate (HDR) brachytherapy works in treating patients with breast cancer that has not spread beyond the breast or the axillary lymph nodes (early-stage) after surgery. Radiation therapy uses a type of energy to kill cancer cells and shrink tumors. Brachytherapy is a type of internal radiation therapy that provides radiation inside the breast to any remaining tumor cells next to the space where the tumor was removed, and is given over a shorter amount of time than standard radiation therapy. Giving accelerated partial breast irradiation (APBI) using high-dose rate (HDR) brachytherapy may reduce the overall time that radiation is delivered to the tumor cells.

Study identification

NCT ID
NCT02526498
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
200 participants

Conditions and interventions

Eligibility (public fields only)

Age range
45 Years and older
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
Jul 14, 2015
Primary completion
Aug 17, 2017
Completion
Mar 30, 2021
Last update posted
May 14, 2023

2015 – 2021

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Arizona Breast Cancer Gilbert Arizona 85297
University of California, San Diego La Jolla California 92093
William Beaumont Hospital Research Institute Royal Oak Michigan 48073
RWJBarnabas Health - Robert Wood Johnson University Hospital New Brunswick New Jersey 08901
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903
Montefiore Medical Center The Bronx New York 10461
21st Centry Oncolgy Yonkers New York 10457
Cleveland Clinic Cleveland Ohio 44106
Bryn Mawr Hospital Bryn Mawr Pennsylvania 19010
Huntsman Cancer Hospital, University of Utah Salt Lake City Utah 84112

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 NCT02526498, 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 May 14, 2023 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02526498 live on ClinicalTrials.gov.

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