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NCT02770586 · ClinicalTrials.gov registry record · NA

Comparison of Positron Emission Mammography and Contrast-enhanced Breast MRI

A NA study, sponsored by Mayo Clinic.

Completed
Registry status
NA
Development phase
50
Enrollment target

NCT02770586: Completed NA study, sponsored by Mayo Clinic.

NCT02770586 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02770586, a NA study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

The hypothesis of this study is that positron emission mammography will provide comparable sensitivity to contrast-enhanced breast MRI in women with a high suspicion of breast cancer. The aim of this study is to determine the sensitivity of Positron Emission Mammography (PEM) relative to that of Contrast-enhanced breast MRI (CE-MRI) in women with a high suspicion of breast cancer

Primary Outcome

The primary analysis is to compare the PEM diagnostic yield to the MRI diagnostic yield, which is considered the standard for this trial. The primary analysis will use the observed MRI diagnostic yield as the control value. The diagnostic yield of PEM will be estimated with a binomial point estimate and corresponding 95% binomial confidence interval (CI). The point estimate for the diagnostic yield (for both MRI and PEM) will be the number of confirmed breast cancers detected by the imaging (i.e

Interventions

  • DIAGNOSTIC_TEST Breast PET

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2015-08
Est. Completion 2019-10-12
Phase NA
Mayo Clinic

2,844 total trials

What the finished NCT02770586 record still lists

NCT02770586 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Breast PET is the first listed.

NCT02770586 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02770586 about?

NCT02770586 is a clinical study titled "Comparison of Positron Emission Mammography and Contrast-enhanced Breast MRI". The hypothesis of this study is that positron emission mammography will provide comparable sensitivity to contrast-enhanced breast MRI in women with a high suspicion of breast cancer. The aim of this study is to determine the sensitivity of Positron Emission Mammography (PEM) relative to that of Co...

What is the current status of trial NCT02770586?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2015-08. Estimated completion is 2019-10-12.

What interventions are being tested in trial NCT02770586?

The interventions under investigation include: Breast PET (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT02770586?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02770586's enrollment target sits among peer trials

50 1279th of 2000 higher than 622 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 NCT02770586, the US trial registry maintained by the National Library of Medicine. NCT02770586 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.