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ACTIVE NOT RECRUITING NA

Tomosynthesis vs. Contrast-Enhanced Mammography in Women With Personal History of Breast Cancer in Western Pennsylvania

NCT04085510 · View on ClinicalTrials.gov ↗

Study Summary

This is a prospective clinical trial that will examine if contrast-enhanced mammography substantially improves breast cancer detection compared to mammography with tomosynthesis, with minimal increase in false-positives, in women with a personal history of breast cancer.

Interventions

  • DEVICE Contrast-enhanced mammogram

Study Locations (3)

Pennsylvania

  • Magee Womancare Passavant Cranberry — Cranberry Township
  • Magee Womancare Monroeville — Monroeville
  • Magee Womens Hospital — Pittsburgh

Trial Details

FieldValue
Enrollment Target 1,647 participants
Start Date 2019-10-23
Est. Completion 2028-12-30
Phase NA

Sponsor

Wendie Berg

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04085510

The ClinicalTrials.gov registry entry for NCT04085510 describes a study currently listed as active not recruiting. 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 1,647 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wendie Berg, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Breast Cancer appearing as the primary indexed condition, and to 1 intervention — of which Contrast-enhanced mammogram 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: NCT04085510 reports 3 study locations spanning 1 distinct geographic area — top geographies include 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 NCT04085510 about?

NCT04085510 is a clinical study titled "Tomosynthesis vs. Contrast-Enhanced Mammography in Women With Personal History of Breast Cancer in Western Pennsylvania". This is a prospective clinical trial that will examine if contrast-enhanced mammography substantially improves breast cancer detection compared to mammography with tomosynthesis, with minimal increase in false-positives, in women with a personal history of breast cancer.

What is the current status of trial NCT04085510?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 1,647 participants. The study started on 2019-10-23. Estimated completion is 2028-12-30.

What conditions does trial NCT04085510 study?

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

What interventions are being tested in trial NCT04085510?

The interventions under investigation include: Contrast-enhanced mammogram (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04085510?

This trial is sponsored by Wendie Berg, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04085510 being conducted?

This trial has 3 study locations across 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