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Spots Global Cancer Trial Database for Using the Conture® Multi-Lumen Balloon to Deliver Accelerated Partial Breast Brachytherapy

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Trial Identification

Brief Title: Using the Conture® Multi-Lumen Balloon to Deliver Accelerated Partial Breast Brachytherapy

Official Title: A Multi-site Prospective, Non Randomized Study Utilizing the Conture® Multi-Lumen Balloon (MLB) Breast Brachytherapy Applicator to Deliver Accelerated Partial Breast Irradiation: Analysis of Dosimetric Success, Local Tumor Control, Cosmetic Outcome, Acute and Chronic Toxicity, and Clinical Scenarios for Optimal Use

Study ID: NCT00699101

Conditions

Breast Cancer

Study Description

Brief Summary: This multiple site, prospective, non-randomized study has been designed to compile information on the efficacy of the Contura™ MLB in delivering APBI in appropriately selected patients through evaluation of dosimetric success as compared with a single central lumen balloon device and through treatment outcomes.

Detailed Description: Data collected during this study will include baseline patient demographics, information related to the time of implant, radiation therapy details, and removal of the device as well as recurrence data, cosmetic outcomes and toxicities. The patient's follow-up data will be collected during the patient's standard follow-up visits.

Eligibility

Minimum Age: 50 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Virginia Commonwealth University, Richmond, Virginia, United States

Contact Details

Name: Douglas W. Arthur, MD

Affiliation: Virginia Commonwealth University

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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