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Using Diagnostic Tools to Stage Breast Cancer

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University of Pennsylvania

Status

Active, not recruiting

Conditions

Breast Cancer

Treatments

Device: MRI, Digital Mammography, Ultrasound and Positron Emission Tomography (PET)

Study type

Interventional

Funder types

Other

Identifiers

NCT00367666
Protocol 414500
NIH funded

Details and patient eligibility

About

This project is aimed at investigating the relative diagnostic and synergy of four state of the art breast imaging techniques (magnetic resonance imaging (MRI), full-field digital mammography (DMAM), ultrasound, and positron emission tomography (PET)) with respect to determining the extent of breast cancer.

Enrollment

400 estimated patients

Sex

Female

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women recently diagnosed with Breast Cancer
  • Will be undergoing surgery (after study) at the Hospital of the University of Pennsylvania

Exclusion criteria

  • Contraindications to MRI
  • previously diagnosed with breast cancer (in the smae breast) within the past 5 years
  • Patients with known locally advanced cancer (prior to study entry) being treated with preoperative adjuvant therapy.
  • Pregnant women

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

400 participants in 1 patient group

Patients Diagnosed with Breast Cancer
Experimental group
Treatment:
Device: MRI, Digital Mammography, Ultrasound and Positron Emission Tomography (PET)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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