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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01681901
Other study ID # OSU-06010
Secondary ID NCI-2012-01176
Status Withdrawn
Phase N/A
First received September 5, 2012
Last updated April 12, 2017
Start date June 7, 2006
Est. completion date April 2007

Study information

Verified date April 2017
Source Ohio State University Comprehensive Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This pilot clinical trial studies ultrasound in detecting lymph node metastasis in older patients with undergoing breast sonography. Diagnostic procedures, such as ultrasound, may help find breast cancer and find out how far the disease has spread


Description:

PRIMARY OBJECTIVES:

I. To develop a reliable and consistent set of guidelines for utilizing diagnostic ultrasound to assess axillary lymph nodes for patient suspicious of breast cancer with possible nodal metastasis.

SECONDARY OBJECTIVES:

I. To explore whether the data collected can be used for pathologic validation of metastatic disease.

OUTLINE:

Patients undergo breast ultrasound.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date April 2007
Est. primary completion date April 2007
Accepts healthy volunteers No
Gender Female
Age group 55 Years and older
Eligibility Inclusion Criteria:

- Patients referred for a breast ultrasound

- Patients who have had a mammogram with a Breast Imaging Reporting and Data System (BIRADS) of >= 4

- Patients who are undiagnosed for breast cancer

Exclusion Criteria:

- Patients who have had breast cancer surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ultrasound imaging
Undergo ultrasound

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University Comprehensive Cancer Center

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of successful evaluations, defined as the consistent capture of the data for geometry, morphology, qualitative vascular information, and quantitative vascular information on 3 axillary lymph nodes The proposed methodology will be considered unfeasible if the proportion of successful evaluations is =< 0.7. at 15 minutes following breast sonogram
Secondary Accuracy of lymph node geometry, measured with a longitudinal and transverse ratio, to determine guidelines for characterizing micro metastases to the lymph nodes Descriptive statistics, such as means, proportions and standard deviations, will be summarized. The longitudinal-transverse ratio will be investigated for cutoff points that yield high sensitivity and to see if results are consistent with prior studies suggesting a ratio of 1.5 or less is indicative of abnormality. The percent agreement between the resulting diagnostic criteria and the surgical/pathological results will be assessed. 3 months
Secondary Accuracy of lymph node morphology, assessed for shape and echogenicity, to determine guidelines for characterizing micro metastases to the lymph nodes Descriptive statistics, such as means, proportions and standard deviations, will be summarized. The percent agreement between the resulting diagnostic criteria and the surgical/pathological results will be assessed. 3 months
Secondary Accuracy of lymph node vascularity, assessed with color doppler, to determine guidelines for characterizing micro metastases to the lymph nodes Descriptive statistics, such as means, proportions and standard deviations, will be summarized. The percent agreement between the resulting diagnostic criteria and the surgical/pathological results will be assessed. 3 months
Secondary Accuracy of lymphatic flow, measured with spectral doppler, to determine guidelines for characterizing micro metastases to the lymph nodes Descriptive statistics, such as means, proportions and standard deviations, will be summarized. The percent agreement between the resulting diagnostic criteria and the surgical/pathological results will be assessed. 3 months
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