Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Lesion Detection of Automated Breast Ultrasound Compared With Handheld Physician-performed Breast Ultrasound

NCT02310776 · View on ClinicalTrials.gov ↗

Study Summary

Compare lesion detection of the automated breast ultrasound (ABVS) exam with the conventional handheld (HH) breast ultrasound (US) exam.

Conditions Studied

Interventions

  • DEVICE Supine automated breast ultrasound scanner
  • DEVICE High-resolution handheld breast ultrasound

Study Locations (2)

Illinois

  • Northwestern Medicine — Chicago

Pennsylvania

  • Weinstein Imaging — Pittsburgh

Trial Details

FieldValue
Enrollment Target 501 participants
Start Date 2012-06
Est. Completion 2015-10
Phase NA

Sponsor

Northwestern University

1,033 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02310776

The ClinicalTrials.gov registry entry for NCT02310776 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 501 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,033 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Breast Diseases appearing as the primary indexed condition, and to 2 interventions — of which Supine automated breast ultrasound scanner is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02310776 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Illinois, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02310776 about?

NCT02310776 is a clinical study titled "Lesion Detection of Automated Breast Ultrasound Compared With Handheld Physician-performed Breast Ultrasound". Compare lesion detection of the automated breast ultrasound (ABVS) exam with the conventional handheld (HH) breast ultrasound (US) exam.

What is the current status of trial NCT02310776?

This trial is currently completed. It is a NA study. The enrollment target is 501 participants. The study started on 2012-06. Estimated completion is 2015-10.

What conditions does trial NCT02310776 study?

This clinical trial studies the following conditions: Breast Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02310776?

The interventions under investigation include: Supine automated breast ultrasound scanner (DEVICE), High-resolution handheld breast ultrasound (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02310776?

This trial is sponsored by Northwestern University, which has 1,033 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02310776 being conducted?

This trial has 2 study locations across Illinois, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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