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TERMINATEDNCT00934297

Visualization Tool for Investigation of Breast Lesions

Magnetic resonance imaging (MRI) is commonly used for the detection of breast lesions in genetically high-risk women due to its high sensitivity. As non-cancerous conditions including normal changes d...

Lead sponsor: Sunnybrook Health Sciences Centre•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Sunnybrook Health Sciences Centre

Age

21 - 80 years

Sex

FEMALE

Healthy Volunteers

No

Inclusion Criteria

•Patients with MRI-identified lesions that cannot be visualized under the second-look ultrasound examination, and who will undergo the recommended unilateral MRI follow-up.

Exclusion Criteria

•US-visible lesion.
•Any contraindications to MRI (e.g., pacemakers, metal implants).
•Any contraindications to US imaging.
•Pregnancy.
•Claustrophobia.
•Inability to lie still for 45 minutes-1 hour.
•In excess of 250 pounds.
•Incapability to provide informed consent.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: July 28, 2011Terms

Trial snapshot

StatusTERMINATED

Phase—

Enrollment10

Start dateJul 2009

Last updatedJul 28, 2011

Condition

Locations shown

Sunnybrook Health Sciences Centre

Toronto, Ontario

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 28, 2011Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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