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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00695968
Other study ID # BRSNSTU0024
Secondary ID 98159BRSNSTU0024
Status Terminated
Phase
First received
Last updated
Start date April 2008
Est. completion date December 2011

Study information

Verified date July 2012
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To determine the sensitivity, specificity, and accuracy of preoperative ultrasound, elastography, mammography and breast MRI in women with dense breast tissue diagnosed with breast cancer; to test whether elastography or MRI can improve upon routine mammogram and conventional ultrasound in women with dense breast tissue.


Recruitment information / eligibility

Status Terminated
Enrollment 9
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:- Patients must have a suspicious breast lesion detected by a physical exam, mammography or U/S . that has not been surgically resected and is being considered to undergo biopsy if clinically indicated.

- Patients must be >= 18 and < 80 years of age, and female.

- Patients must have the ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:- Patients who have already had primary surgical excision of the suspicious finding

- <18 or >80 years of age

- Pregnant or Lactating Women

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

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