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Completed Phase 2 Interventional Results available

MammoSite as Sole Radiation Therapy Technique for Ductal Carcinoma In-Situ

ClinicalTrials.gov ID: NCT00586326

Public ClinicalTrials.gov record NCT00586326. 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 4, 2026, 5:05 PM EDT

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

Official title

MammoSite Radiation Therapy System (RTS) as the Sole Radiation Therapy Technique for Ductal Carcinoma In-Situ (DCIS)

Brief summary

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

This study has been designed to compile information on the efficacy of the MammoSite RTS providing sole radiation therapy for patients with pure DCIS.

Study identification

NCT ID
NCT00586326
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hologic, Inc.
Industry
Enrollment
133 participants

Conditions and interventions

Conditions

Interventions

Device

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 31, 2003
Primary completion
Dec 31, 2005
Completion
Mar 31, 2011
Last update posted
Nov 5, 2012

2003 – 2011

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Arizona Oncology Services Phoenix Arizona 85032
Daniel Freeman Hospital Inglewood California 90301
University of Southern California Los Angeles California 90033
Cedars Medical Center Miami Beach Florida 33136
St. Agnes Hospital Baltimore Maryland 21229
William Beaumont Hospital Royal Oak Michigan 48073
NY Presbyterian New York New York 10065
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Rhode Island Hospital Providence Rhode Island 02903
MD Anderson Cancer Clinic Houston Texas 77030
Virginia Commonwealth University Richmond Virginia 23298
Swedish Cancer Institute Seattle Washington 98104

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 NCT00586326, 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 Nov 5, 2012 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00586326 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →