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NCT05408260 · ClinicalTrials.gov registry record · NA

A Study to Compare the Effectiveness of Two Types of Ultrasound Technologies in Women Who Have Had Breast Cancer

A NA study, sponsored by Thomas Jefferson University.

Completed
Registry status
NA
Development phase
12
Enrollment target

NCT05408260: Completed NA study, sponsored by Thomas Jefferson University.

NCT05408260 is a NA study that has completed, run by Thomas Jefferson University. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05408260, a NA study, has completed, sponsored by Thomas Jefferson University.

COMPLETED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

This clinical trial evaluates automated breast ultrasound (ABUS) and handheld ultrasound (HHUS) for the screening of women who have undergone breast reconstruction after breast cancer. Ultrasounds use high-frequency sound waves to create pictures of internal organs and tissues. ABUS has been found to be equal to HHUS for whole breast screening, but no data exist on its use for screening of reconstructed patients. This clinical trial evaluates the feasibility of using ABUS versus HHUS to screen women who have undergone reconstruction.

Primary Outcome

This is a binary endpoint. The rate of artifact will be compared between handheld and automated scanning using McNemar test.

Interventions

  • PROCEDURE Ultrasonography
  • PROCEDURE Automated Breast Ultrasound

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2022-11-18
Est. Completion 2025-02-17
Phase NA
Thomas Jefferson University

292 total trials

What the finished NCT05408260 record still lists

NCT05408260 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Ultrasonography is the first listed.

NCT05408260 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05408260 about?

NCT05408260 is a clinical study titled "A Study to Compare the Effectiveness of Two Types of Ultrasound Technologies in Women Who Have Had Breast Cancer". This clinical trial evaluates automated breast ultrasound (ABUS) and handheld ultrasound (HHUS) for the screening of women who have undergone breast reconstruction after breast cancer. Ultrasounds use high-frequency sound waves to create pictures of internal organs and tissues. ABUS has been found t...

What is the current status of trial NCT05408260?

This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2022-11-18. Estimated completion is 2025-02-17.

What interventions are being tested in trial NCT05408260?

The interventions under investigation include: Ultrasonography (PROCEDURE), Automated Breast Ultrasound (PROCEDURE).

Who is sponsoring clinical trial NCT05408260?

This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05408260's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05408260, the US trial registry maintained by the National Library of Medicine. NCT05408260 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.