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NCT01060085 · ClinicalTrials.gov registry record

Digital Breast Tomosynthesis Versus Contrast Enhanced Magnetic Resonance Imaging (MRI) for Breast Cancer Staging

A clinical trial of Invasive Breast Cancer and Ductal Carcinoma In Situ, sponsored by Dartmouth-Hitchcock Medical Center.

Completed
Registry status
51
Enrollment target
1
Study location

NCT01060085 is a study of Invasive Breast Cancer and Ductal Carcinoma In Situ that has completed, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 51 participants, below the 130-participant average among 19 other Invasive Breast Cancer trials with a reported enrollment target (61% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01060085, a study of Invasive Breast Cancer and Ductal Carcinoma In Situ, has completed, sponsored by Dartmouth-Hitchcock Medical Center.

COMPLETED
Registry status
51 participants
Enrollment target
1
Study location

Study Summary

The primary objective of this study is to compare the diagnostic accuracy of Digital Breast Tomosynthesis (DBT) versus that of Contrast Enhanced Magnetic Resonance Imaging (CEMRI) in determining the size of breast cancer preoperatively. Secondary objectives include: 1. Comparing the operating characteristics of each combined imaging protocol with respect to the reference standard, i.e. histopathologic assessment, of additional non-index lesions. 2. Comparison of re-excision rates based on estimated disease extent from adjunctive CEMRI vs. adjunctive DBT. 3. Evaluation of patient satisfaction with regard to the adjunctive modality (DBT vs. CEMRI).

Study Locations (1)

New Hampshire

  • Dartmouth-Hitchcock Medical Center - Lebanon

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2009-02
Est. Completion 2016-12-31

Sponsor

Dartmouth-Hitchcock Medical Center

427 total trials

What the Registry Record Tells You About NCT01060085

The ClinicalTrials.gov registry entry for NCT01060085 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 130-participant average among 19 other Invasive Breast Cancer trials with a reported enrollment target (61% lower). The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 427 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Invasive Breast Cancer appearing as the primary indexed condition, and to 0 interventions.

NCT01060085 reports 1 study location spanning 1 distinct geographic area - top geographies include New Hampshire.

Frequently Asked Questions

What is clinical trial NCT01060085 about?

NCT01060085 is a clinical study titled "Digital Breast Tomosynthesis Versus Contrast Enhanced Magnetic Resonance Imaging (MRI) for Breast Cancer Staging". The primary objective of this study is to compare the diagnostic accuracy of Digital Breast Tomosynthesis (DBT) versus that of Contrast Enhanced Magnetic Resonance Imaging (CEMRI) in determining the size of breast cancer preoperatively. Secondary objectives include: 1. Comparing the operating char...

What is the current status of trial NCT01060085?

This trial is currently completed. The enrollment target is 51 participants. The study started on 2009-02. Estimated completion is 2016-12-31.

What conditions does trial NCT01060085 study?

This clinical trial studies the following conditions: Invasive Breast Cancer, Ductal Carcinoma In Situ.

Who is sponsoring clinical trial NCT01060085?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01060085 being conducted?

This trial has 1 study location across New Hampshire. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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