PET Imaging to Determine the Role of PET in the Assessment of Regional Disease in Breast Cancer (PET PREDICT Trial)
NCT00201942 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 336
Last updated 2007-10-18
Summary
The overall goal of this study is to determine how FDG-PET can be incorporated into the assessment of the axilla in the staging and treatment of women with early stage breast cancer.
A multicentre, prospective, diagnostic accuracy study will be conducted evaluating the ability of positronic emission tomography using fluorodeoxyglucose (FDG-PET) to detect the presence or absence of axillary lymph node metastases in newly diagnosed breast cancer patients with no clinical evidence of spread of disease beyond the breast.
Conditions
Interventions
- PROCEDURE
-
PET scan
Sponsors & Collaborators
-
Ontario Ministry of Health and Long Term Care
collaborator OTHER_GOV -
Ontario Clinical Oncology Group (OCOG)
lead OTHER
Principal Investigators
-
Kathleen Pritchard, MD · Sunnybrook Regional Cancer Centre
-
Claire Holloway, MD · Sunnybrook Regional Cancer Centre
-
David McCready, MD · Princess Margaret Hospital, Canada
-
Jim Julian, M.Math. · McMaster University
-
Mark N Levine, MD · Ontario Clinical Oncology Group (OCOG)
-
Wendy Shelley, MD · Kingston Regional Cancer Centre
-
Karen Gulenchyn, MD, PhD · McMaster University
-
Frances O'Malley, MD · MOUNT SINAI HOSPITAL
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-02-28
- Completion
- 2007-05-31
Countries
- Canada
Study Locations
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