The PREDICT Registry:

Description

This is a prospective, non-interventional (observational) cohort study conducted within the medical network of the participating investigators and institutions. Patients meeting the eligibility criteria (see below) will be eligible for participation and the investigators will obtain written informed consent. A central Institutional Review Board (IRB), WCG IRB, will approve the protocol and each participating institution.

Conditions

DCIS

Study Overview

Study Details

Study overview

This is a prospective, non-interventional (observational) cohort study conducted within the medical network of the participating investigators and institutions. Patients meeting the eligibility criteria (see below) will be eligible for participation and the investigators will obtain written informed consent. A central Institutional Review Board (IRB), WCG IRB, will approve the protocol and each participating institution.

A Prospective Registry Study to Evaluate the Effect of the DCISionRT Test on Treatment Decisions in Patients with DCIS Following Breast Conserving Therapy

The PREDICT Registry:

Condition
DCIS
Intervention / Treatment

-

Contacts and Locations

Phoenix

Arizona Center for Cancer Care, Phoenix, Arizona, United States, 85027

Sacramento

Sutter Institute for Medical Research, Sacramento, California, United States, 95816

San Mateo

Mills-Peninsula Medical Center, San Mateo, California, United States, 94019

Aurora

University of Colorado Denver, Aurora, Colorado, United States, 80045

Colorado Springs

UC Health - Memorial Hospital, Colorado Springs, Colorado Springs, Colorado, United States, 80909

Tampa

St. Joseph's Hospital Tampa, Tampa, Florida, United States, 33614

Boston

Dana-Farber Cancer Institute, Boston, Massachusetts, United States, 02115

South Weymouth

Dana-Farber/Brigham and Women's Cancer Center at South Shore, South Weymouth, Massachusetts, United States, 02190

Troy

Comprehensive Breast Care, Troy, Michigan, United States, 48098

Brooklyn

Maimonides Cancer Center, Brooklyn, New York, United States, 11220

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    30 Years to 85 Years

    Sexes Eligible for Study

    FEMALE

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    PreludeDx,

    Troy Bremer, PhD, PRINCIPAL_INVESTIGATOR, PreludeDx

    Pat W Whitworth, MD, STUDY_CHAIR, PreludeDx

    Rachel Rabinovitch, MD, STUDY_CHAIR, University of Colorado, Denver

    Pat Borgen, MD, STUDY_CHAIR, Maimonides Medical Center

    Study Record Dates

    2035-12